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ParaPRO

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uuid000jqzl

Namestring
ParaPRO
Legal namestring
ParaPRO, LLC
Websiteurl
parapro.com
Company typeenum
Private
Founded yearint
2002
Descriptiontext

ParaPRO, LLC is a privately-held specialty pharmaceutical company headquartered in Carmel, Indiana, founded in 2002 under a licensing agreement with Eli Lilly to commercialize the naturally-derived anti-parasitic compound spinosad for human clinical uses. The company has built its business around a single asset class — topical spinosad formulations — with Natroba (spinosad) Topical Suspension 0.9% as the centerpiece product. Natroba received FDA approval in 2011 as a prescription treatment for head lice in patients six months of age and older, and is positioned against the documented 98.3% resistance of head lice to pyrethroid-based OTC products across 48 US states. The product targets the layer of the skin where lice reside (the stratum corneum) and is not systemically absorbed, allowing a 10-minute application time with a differentiated mechanism of action.

The company monetizes through branded prescription sales of Natroba and, more recently, an Authorized Generic (Spinosad Topical Suspension 0.9%) marketed via the SpinosadRx storefront. Go-to-market is an enterprise field-sales model: pharmaceutical representatives conduct 40-65 unique office visits per week targeting pediatricians, family physicians, NPs, PAs, and school nurses, supported by partnerships with NASN and AAFP. The product is reported as the most often prescribed Rx medication in the head lice category and is prescribed by an estimated three in five pediatricians. End consumers are families with school-aged children, with treatment failure (often after multiple OTC attempts) driving Rx conversion.

The R&D pipeline centers on extending spinosad into a second indication, with a Phase 3 randomized, double-blind, placebo-controlled study underway for scabies conducted in collaboration with Concentrics Research. ParaPRO is a family-controlled private company led by William Culpepper II (CEO) and William Culpepper III (President), with the proprietary spinosad intellectual property originating from Eli Lilly and earning a Presidential Green Chemistry Award from the EPA. The company operates exclusively in the United States, has no institutional investor or parent-company backing disclosed, and runs a focused product portfolio centered on anti-parasitic topical therapy.

Short descriptiontext

ParaPRO is a private US specialty pharmaceutical company that develops and commercializes prescription topical spinosad treatments, primarily Natroba, an FDA-approved head-lice therapy sold to pediatricians, family physicians, and families across the United States.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersCarmel, United States
HQ citystring
Carmel
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
specialty pharmaceuticals, antiparasitic therapies, prescription pediculicides, topical head lice treatments, spinosad formulations
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Medicinal Chemicals & Botanical Products2833
Product category
Specialty Pharmaceuticals (Antiparasitic Therapeutics)
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Prescription Pharmaceutical Sales
TypeOne Time License
Description

ParaPRO commercializes Natroba (spinosad) Topical Suspension 0.9% as an FDA-approved prescription medication for head lice. Revenue is generated through prescription sales to patients via pharmacies and healthcare providers, with the product being the most widely prescribed in its category.

parapro.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Marketing or Sales, Personnel, Supply Chain, Technology or R&D, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Natroba
Description

Natroba (spinosad) Topical Suspension, 0.9% - FDA-approved prescription treatment for head lice infestations in patients six months of age and older.

parapro.com
+1 more record
Core offering1 text field

ParaPRO develops and commercializes prescription topical therapeutics for parasite infestations, with a portfolio centered on the spinosad compound. The lead product, Natroba (spinosad) Topical Suspension 0.9%, is an FDA-approved prescription treatment for head lice infestations in patients six months of age and older, and is the most often prescribed Rx medication in its category. The company also markets an Authorized Generic version (Spinosad Topical Suspension 0.9%) to broaden patient access, and is developing an investigational spinosad-based treatment for scabies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 98.3% resistance rate to pyrethroid and permethrin-based OTC treatments in 48 states
+3 more records
Product overview1 text field

ParaPRO is a specialty pharmaceutical company offering a focused portfolio centered on spinosad-based topical treatments for parasitic infestations. The primary product is Natroba (spinosad) Topical Suspension 0.9%, an FDA-approved prescription medication for head lice in patients 6 months and older, which is the most widely prescribed in its category. The company also offers an Authorized Generic version (Spinosad Topical Suspension 0.9%) to improve patient access. Spinosad, the active compound, is a naturally occurring anti-parasitic agent derived from soil microorganisms that targets parasites in the stratum corneum without systemic absorption. The company is also developing investigational treatments for scabies.

Product and service2 records
1Natroba (spinosad) Topical Suspension, 0.9%
CategoryPrescription pediculicide (head lice treatment)
Description

FDA-approved prescription pediculicide for the topical treatment of head lice infestations in patients six months of age and older. Contains spinosad 0.9% as the active ingredient, applied for 10 minutes, and is the most often prescribed Rx medication in the head lice category.

2Spinosad Topical Suspension, 0.9% (Authorized Generic)
CategoryAuthorized generic prescription pediculicide
Description

Authorized generic version of Natroba marketed as Spinosad Topical Suspension 0.9% to broaden patient and family access to the spinosad-based head lice treatment.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2002-01-01
Description

ParaPRO was established in 2002 through an agreement with Eli Lilly to commercialize the spinosad compound for human clinical uses. This licensing agreement is the foundation of the company's business.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Partnership with NASN to support the broader professional community and bring about better outcomes for children and families affected by head lice infestations.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Partnership with AAFP to bring about better outcomes for children and families and support the professional community with insights, tools, and resources.

Strategic tierMinorTypeImplementation/ SI/ Consulting Partner
Description

Concentrics Research conducted ParaPRO's Phase 3, Randomized, Double Blind, Placebo-Controlled Study to assess the safety, efficacy and pharmacokinetics of the investigational product for the treatment of scabies.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Large dermatology-focused pharmaceutical company with overlapping antiparasitic and topical franchises, serving the same prescriber base as ParaPRO but with a much broader portfolio across acne, rosacea, and skin health.

TypeDirect peer
Description

Specialty pharma that markets Rx head lice treatments including Sklice (ivermectin 0.5%), directly competing with Natroba for the same pediatric and family practice prescribers and patient population.

TypeDirect peer
Description

Niche specialty pharmaceutical company with a focused portfolio of FDA-approved topical prescription therapies (e.g., Ycanth) for skin conditions, sharing ParaPRO's model of a small commercial organization targeting prescribers in a single dermatologic/parasitic indication.

TypeBroad incumbent
Description

Privately held specialty pharmaceutical company with comparable scale and family-ownership profile, operating in adjacent pediatric and women's health categories using a similar field-sales-driven Rx commercialization model.

TypeOthers
Description

Bayer's Rid brand is a leading OTC head lice treatment, representing the OTC competitive front that ParaPRO's Rx alternative must reach via pediatrician and family practice referrals after multiple OTC failures.

TypeOthers
Description

Consumer health company whose Nix brand is the leading OTC head lice treatment in the US, representing the OTC-first competitive dynamic that ultimately funnels treatment-failure patients toward Rx options like Natroba.

TypeBroad incumbent
Description

Specialty pharmaceutical company with a pediatric and rare disease focus that shares ParaPRO's commercial model of small, focused sales forces targeting prescribers in niche indications.

TypeBroad incumbent
Description

Specialty and generic topical pharmaceutical company with deep expertise in skin-directed Rx products, providing a comparable benchmark for niche topical Rx commercialization and authorized generic strategies.

TypeEmerging player
Description

Emerging dermatology specialty pharmaceutical company with a focused portfolio of topical prescription therapies (e.g., Zoryve), sharing ParaPRO's lean commercial approach to single-indication dermatologic categories.

TypeBroad incumbent
Description

Specialty and generic pharmaceutical company with relevant dermatology and women's health Rx portfolios, providing a comparable size and business model benchmark for niche Rx commercialization in the US.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

ParaPRO

Specialty Pharmaceuticals (Antiparasitic Therapeutics)parapro.com

ParaPRO is a private US specialty pharmaceutical company that develops and commercializes prescription topical spinosad treatments, primarily Natroba, an FDA-approved head-lice therapy sold to pediatricians, family physicians, and families across the United States.

What ParaPRO does

ParaPRO, LLC is a privately-held specialty pharmaceutical company headquartered in Carmel, Indiana, founded in 2002 under a licensing agreement with Eli Lilly to commercialize the naturally-derived anti-parasitic compound spinosad for human clinical uses. The company has built its business around a single asset class — topical spinosad formulations — with Natroba (spinosad) Topical Suspension 0.9% as the centerpiece product. Natroba received FDA approval in 2011 as a prescription treatment for head lice in patients six months of age and older, and is positioned against the documented 98.3% resistance of head lice to pyrethroid-based OTC products across 48 US states. The product targets the layer of the skin where lice reside (the stratum corneum) and is not systemically absorbed, allowing a 10-minute application time with a differentiated mechanism of action.

The company monetizes through branded prescription sales of Natroba and, more recently, an Authorized Generic (Spinosad Topical Suspension 0.9%) marketed via the SpinosadRx storefront. Go-to-market is an enterprise field-sales model: pharmaceutical representatives conduct 40-65 unique office visits per week targeting pediatricians, family physicians, NPs, PAs, and school nurses, supported by partnerships with NASN and AAFP. The product is reported as the most often prescribed Rx medication in the head lice category and is prescribed by an estimated three in five pediatricians. End consumers are families with school-aged children, with treatment failure (often after multiple OTC attempts) driving Rx conversion.

The R&D pipeline centers on extending spinosad into a second indication, with a Phase 3 randomized, double-blind, placebo-controlled study underway for scabies conducted in collaboration with Concentrics Research. ParaPRO is a family-controlled private company led by William Culpepper II (CEO) and William Culpepper III (President), with the proprietary spinosad intellectual property originating from Eli Lilly and earning a Presidential Green Chemistry Award from the EPA. The company operates exclusively in the United States, has no institutional investor or parent-company backing disclosed, and runs a focused product portfolio centered on anti-parasitic topical therapy.

ParaPRO firmographics

Firmographics
Name
ParaPRO
Legal name
ParaPRO, LLC
Website
https://parapro.com
Company type
Private
Founded year
2002
Operating status
Operating
Headcount range
101–250 employees
Short description
ParaPRO is a private US specialty pharmaceutical company that develops and commercializes prescription topical spinosad treatments, primarily Natroba, an FDA-approved head-lice therapy sold to pediatricians, family physicians, and families across the United States.
Ownership category
akta.pro rank

Where ParaPRO is headquartered

Location

Headquarters

HQ city
Carmel
HQ country
United States
HQ region
North America

Offices1 record

Markets served

ParaPRO business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Marketing or Sales, Personnel, Supply Chain, Technology or R&D, Operations

Revenue model

  1. Prescription Pharmaceutical Sales: ParaPRO commercializes Natroba (spinosad) Topical Suspension 0.9% as an FDA-approved prescription medication for head lice. Revenue is generated through prescription sales to patients via pharmacies and healthcare providers, with the product being the most widely prescribed in its category.

Go-to-market motion1 record

Distribution channels2 records

Marketing channels4 records

ParaPRO product offering

Product offering

Core offering

ParaPRO develops and commercializes prescription topical therapeutics for parasite infestations, with a portfolio centered on the spinosad compound. The lead product, Natroba (spinosad) Topical Suspension 0.9%, is an FDA-approved prescription treatment for head lice infestations in patients six months of age and older, and is the most often prescribed Rx medication in its category. The company also markets an Authorized Generic version (Spinosad Topical Suspension 0.9%) to broaden patient access, and is developing an investigational spinosad-based treatment for scabies.

Product overview

ParaPRO is a specialty pharmaceutical company offering a focused portfolio centered on spinosad-based topical treatments for parasitic infestations. The primary product is Natroba (spinosad) Topical Suspension 0.9%, an FDA-approved prescription medication for head lice in patients 6 months and older, which is the most widely prescribed in its category. The company also offers an Authorized Generic version (Spinosad Topical Suspension 0.9%) to improve patient access. Spinosad, the active compound, is a naturally occurring anti-parasitic agent derived from soil microorganisms that targets parasites in the stratum corneum without systemic absorption. The company is also developing investigational treatments for scabies.

Differentiator

Problem solved

Functional benefit

Brands

  • Natroba: Natroba (spinosad) Topical Suspension, 0.9% - FDA-approved prescription treatment for head lice infestations in patients six months of age and older.
  • Spinosad Topical Suspension, 0.9%

Products and services

  • Natroba (spinosad) Topical Suspension, 0.9% FDA-approved prescription pediculicide for the topical treatment of head lice infestations in patients six months of age and older. Contains spinosad 0.9% as the active ingredient, applied for 10 minutes, and is the most often prescribed Rx medication in the head lice category.
  • Spinosad Topical Suspension, 0.9% (Authorized Generic) Authorized generic version of Natroba marketed as Spinosad Topical Suspension 0.9% to broaden patient and family access to the spinosad-based head lice treatment.

Quantifiable outcome

  • 98.3% resistance rate to pyrethroid and permethrin-based OTC treatments in 48 states
  • +3 more outcomes

Companies that use ParaPRO

Customer profile

Segments3 records

Ideal customer profiles2 records

ParaPRO technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

ParaPRO partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Eli LillycoreOEM/ Whitelabel/ Licensing Partner · 1 January 2002ParaPRO was established in 2002 through an agreement with Eli Lilly to commercialize the spinosad compound for human clinical uses. This licensing agreement is the foundation of the company's business.
  • National Association of School Nurses (NASN)coreStrategic or Co-development PartnerPartnership with NASN to support the broader professional community and bring about better outcomes for children and families affected by head lice infestations.
  • American Academy of Family Physicians (AAFP)coreStrategic or Co-development PartnerPartnership with AAFP to bring about better outcomes for children and families and support the professional community with insights, tools, and resources.
  • Concentrics ResearchminorImplementation/ SI/ Consulting PartnerConcentrics Research conducted ParaPRO's Phase 3, Randomized, Double Blind, Placebo-Controlled Study to assess the safety, efficacy and pharmacokinetics of the investigational product for the treatment of scabies.

Scale indicators4 records

Recent moves5 records

Expansion highlights4 records

ParaPRO competitors and assessment

Company assessment

Broad incumbents

  • Galderma: Large dermatology-focused pharmaceutical company with overlapping antiparasitic and topical franchises, serving the same prescriber base as ParaPRO but with a much broader portfolio across acne, rosacea, and skin health.
  • Mission Pharmacal: Privately held specialty pharmaceutical company with comparable scale and family-ownership profile, operating in adjacent pediatric and women's health categories using a similar field-sales-driven Rx commercialization model.
  • Aytu BioPharma: Specialty pharmaceutical company with a pediatric and rare disease focus that shares ParaPRO's commercial model of small, focused sales forces targeting prescribers in niche indications.
  • Padagis: Specialty and generic topical pharmaceutical company with deep expertise in skin-directed Rx products, providing a comparable benchmark for niche topical Rx commercialization and authorized generic strategies.
  • Mayne Pharma: Specialty and generic pharmaceutical company with relevant dermatology and women's health Rx portfolios, providing a comparable size and business model benchmark for niche Rx commercialization in the US.

Direct peers

  • Azurity Pharmaceuticals: Specialty pharma that markets Rx head lice treatments including Sklice (ivermectin 0.5%), directly competing with Natroba for the same pediatric and family practice prescribers and patient population.
  • Verrica Pharmaceuticals: Niche specialty pharmaceutical company with a focused portfolio of FDA-approved topical prescription therapies (e.g., Ycanth) for skin conditions, sharing ParaPRO's model of a small commercial organization targeting prescribers in a single dermatologic/parasitic indication.

Others

  • Bayer Consumer Health: Bayer's Rid brand is a leading OTC head lice treatment, representing the OTC competitive front that ParaPRO's Rx alternative must reach via pediatrician and family practice referrals after multiple OTC failures.
  • Church & Dwight: Consumer health company whose Nix brand is the leading OTC head lice treatment in the US, representing the OTC-first competitive dynamic that ultimately funnels treatment-failure patients toward Rx options like Natroba.

Emerging players

  • Arcutis Biotherapeutics: Emerging dermatology specialty pharmaceutical company with a focused portfolio of topical prescription therapies (e.g., Zoryve), sharing ParaPRO's lean commercial approach to single-indication dermatologic categories.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

ParaPRO social profiles

Digital presence

ParaPRO financial estimates

Financial estimate

Revenue estimate

Valuation estimate

ParaPRO leadership team

Management profile

Number of profiles

Profiles6 records

ParaPRO funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

ParaPRO M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about ParaPRO

What does ParaPRO do?

ParaPRO develops and commercializes prescription topical therapeutics for parasite infestations, with a portfolio centered on the spinosad compound. The lead product, Natroba (spinosad) Topical Suspension 0.9%, is an FDA-approved prescription treatment for head lice infestations in patients six months of age and older, and is the most often prescribed Rx medication in its category. The company also markets an Authorized Generic version (Spinosad Topical Suspension 0.9%) to broaden patient access, and is developing an investigational spinosad-based treatment for scabies.

Is ParaPRO a public or private company?

ParaPRO is a private company. It is classified as family owned and is currently operating.

When was ParaPRO founded?

ParaPRO was founded in 2002. It employs 101 to 250 people.

Where is ParaPRO based?

ParaPRO is headquartered in Carmel, United States, in the North America region.

How does ParaPRO make money?

One revenue line is on record: prescription Pharmaceutical Sales.

Who are ParaPRO's main competitors?

Broad incumbents on record are Galderma, Mission Pharmacal, Aytu BioPharma, Padagis and Mayne Pharma. Direct peers are Azurity Pharmaceuticals and Verrica Pharmaceuticals. Others are Bayer Consumer Health and Church & Dwight. Arcutis Biotherapeutics is listed as an emerging player.

Does ParaPRO have an API?

No public API is recorded for ParaPRO.

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Live signals
PR NewswirePARAPRO'S THOUGHT LEADER AI: WHERE ARTIFICIAL INTELLIGENCE MEETS SCABIES EXPERTISEParaPRO, a specialty pharmaceutical company specializing in treatments for human ectoparasites, has launched Thought Leader AI, an AI-driven virtual consultation platform developed in collaboration with the Institute for Creative Technologies at the University of Southern California.PR NewswirePARAPRO INTRODUCES THE FIRST AI-BASED INTERACTIVE MEDICAL EDUCATION PLATFORM AT THE AMERICAN ACADEMY OF PEDIATRICS NATIONAL CONFERENCE AND EXHIBITIONParaPRO, a specialty pharmaceutical company based in Carmel, Indiana, announced the launch of Thought Leader AI — the first AI-based interactive medical education platform enabling healthcare practitioners to engage in real-time conversations with digital human avatars of clinical experts — at the American Academy of Pediatrics National Conference in Anaheim, California. The platform, developed in collaboration with the University of Southern California Institute for Creative Technologies, was introduced alongside the company's FDA-approved treatment for scabies, addressing the common misdiagnosis and mistreatment of the condition. The company positions the technology as a new paradigm for scientific exchange and medical education, allowing prescribers to interact with expert avatars regardless of physical barriers.PR NewswireLeading Expert On Head Lice Urges Parents To Follow The Science When Treating InfestationsParaPRO LLC, a specialty pharmaceutical company focused on anti-parasitic treatments, and Dr. John Clark of the University of Massachusetts Amherst are urging parents to consult healthcare providers for head lice treatment amid widespread resistance to over-the-counter products. A landmark study cited in the release found that 98.3% of surveyed U.S. head lice have become genetically resistant to pyrethrin- and permethrin-based OTC treatments. The release promotes telemedicine as an alternative for families and criticizes both government agencies and pharmacy retailers for continuing to recommend and sell products with reduced efficacy.European Medical JournalRedHill Biopharma Initiates Promotion of Esomeprazole Strontium Delayed-Release Capsules 49.3 mg in the U.S.RedHill Biopharma has initiated the promotion of Esomeprazole Strontium Delayed-Release Capsules 49.3 mg in the United States through its specialized gastrointestinal sales force. The company holds exclusive promotion rights under a revenue-sharing agreement with ParaPRO LLC for this FDA-approved proton pump inhibitor indicated for GERD and other GI conditions.