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National Rosacea Society

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Namestring
National Rosacea Society
Legal namestring
National Rosacea Society
Websiteurl
rosacea.org
Company typeenum
Private
Founded yearint
1992
Descriptiontext

The National Rosacea Society (NRS) is a 501(c)(3) nonprofit patient-advocacy organization founded in 1992 and headquartered in Chicago, Illinois. Its mission is to improve outcomes for the estimated 16 million Americans and 415 million people worldwide affected by rosacea by raising disease awareness, providing free education, and funding medical research. The NRS primarily serves rosacea patients and a secondary audience of dermatologists, physicians, and eye-care specialists who rely on its clinical tools and patient handouts. With 1–10 employees, the organization operates a community-led model anchored by rosacea.org, the quarterly Rosacea Review newsletter, an annual April Rosacea Awareness Month campaign, and presence across Facebook, Instagram, Twitter, Pinterest, Bluesky, LinkedIn, and YouTube.

The NRS's core deliverables are content-based rather than technology-based. Its product set comprises patient education booklets (Understanding Rosacea, Coping with Rosacea, Managing Rosacea, Recognizing Redness, and the 2026-updated Rosacea Diary), the Seal of Acceptance certification program for rosacea-friendly skin care and cosmetics (currently covering 50+ products), the Rosacea Review newsletter (published since 1996), physician resources including clinical scorecards and treatment algorithms, and a Research Grants Program that has been funding rosacea research for 26 consecutive years. All materials are distributed free of charge via downloadable PDFs, email, postal mail, and bulk distribution to medical practices. No proprietary technology platform, mobile app, or AI/ML capability is offered.

The organization's funding model is dual-track. The first stream is individual donations and membership fees from patients and supporters. The second stream is unrestricted educational grants from pharmaceutical, dermatology, medical-device, and cosmetics companies — six of which are named for the 2026 website-maintenance cycle: Journey Medical, Mayne Pharma, Crescel, Sente Labs, Laura Geller, and Cutera. There are no shareholders, parent company, or venture capital involvement; governance is provided by a Board of Directors and a Medical Advisory Board, and leadership is exercised through a small editorial and program team including a Managing Editor, an Editor (who also serves as president of Dermatology and Skin Care Center of Birmingham), and a Social Media Editor.

Short descriptiontext

The National Rosacea Society is a 501(c)(3) nonprofit founded in 1992 and headquartered in Chicago that provides free rosacea education, patient materials, physician resources, and research grants to rosacea patients and healthcare professionals, funded by donations and pharmaceutical educational grants.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersChicago, United States
HQ citystring
Chicago
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
rosacea patient education, medical research grants, patient advocacy nonprofit, skin condition awareness, seal of acceptance certification
Industry1 code
1Sensitive Skin & Rosacea-Calming Treatments
CodeHSALADAFPrimaryYes
NAICS code1 code
  • Professional Organizations813920
SIC code1 code
  • Services-Membership Organizations8600
Product category
Patient Advocacy / Nonprofit Health Organization
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Donations and Membership
TypeOthers
Description

The organization collects individual donations and membership fees from patients and supporters to fund research grants and public education programs.

rosacea.org
2Pharmaceutical Company Educational Grants
TypeProfessional Services
Description

Website maintenance is supported by unrestricted educational grants from pharmaceutical and dermatology companies including Journey Medical, Mayne Pharma, Crescel, Sente Labs, Laura Geller, and Cutera.

rosacea.org
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components4 values
Personnel, Marketing or Sales, Operations, Others
GTM typeB2C
B2C
Offering typeServices
Services
Core offering1 text field

The National Rosacea Society (NRS) is a 501(c)(3) nonprofit organization that provides free educational resources to rosacea patients, funds medical research into the cause and treatment of rosacea, and runs a Seal of Acceptance program that certifies skin care and cosmetic products deemed appropriate for sensitive rosacea-prone skin.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

The National Rosacea Society operates primarily as an educational and awareness organization rather than a technology product company. Its core offerings consist of patient education materials including the Rosacea Diary (updated 2026), Understanding Rosacea Brochure, Coping with Rosacea Brochure, Managing Rosacea Brochure, and Recognizing Redness Booklet. The society also runs a Seal of Acceptance Program that certifies skin care and cosmetic products as suitable for rosacea patients. Additionally, it publishes the Rosacea Review Newsletter and funds medical research through its Research Grants Program.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Dermatology research funding nonprofit awarding grants to advance skin science. Direct peer on the research-grants vertical of NRS's mission, with similar donor and industry funding architecture.

TypeOthers
Description

Professional research society for dermatology investigators. Relevant adjacency for NRS's research grants program and scientific advisory operations, though it serves investigators rather than patients directly.

TypeDirect peer
Description

Patient advocacy nonprofit for eczema, operating a near-identical model of patient education, physician resources, research grants, and disease-specific awareness campaigns. Direct structural and operational analogue to NRS.

TypeDirect peer
Description

Chronic disease patient advocacy nonprofit with similar operational scale, pharma grant reliance, and member/donor-driven education model. Comparable build of patient resources, physician tools, and research programming.

TypeDirect peer
Description

Patient advocacy nonprofit for asthma and allergies with analogous chronic-condition awareness, education, research funding, and pharma sponsorship model. Comparable scale and operational footprint.

6American Autoimmune Related Diseases Association
TypeOthers
Description

Umbrella advocacy organization for autoimmune diseases. Thematically adjacent to NRS as a chronic-condition advocacy model, useful for comparison on coalition-style fundraising and cross-disease awareness.

TypeDirect peer
Description

Skin disease advocacy nonprofit focused on awareness, education, and physician resources. Mirrors NRS's content-library, awareness-month, and physician outreach playbook in a different skin condition.

TypeDirect peer
Description

Skin health advocacy nonprofit combining research funding and public education. Closely comparable mission, structure, and donor base to NRS, though broader across dermatologic conditions.

TypeBroad incumbent
Description

Largest professional dermatology association in the US, with far broader physician engagement, CME, and patient education capabilities. Overlaps with NRS on rosacea physician resources but operates as a multi-disease umbrella.

TypeDirect peer
Description

Patient advocacy nonprofit for psoriasis with patient education, support resources, research funding, and a comparable donor/pharma sponsorship model. Closest peer in scale and mission within dermatology.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

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

Ideal customer profile4 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

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 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 →

National Rosacea Society

Patient Advocacy / Nonprofit Health Organizationrosacea.org

The National Rosacea Society is a 501(c)(3) nonprofit founded in 1992 and headquartered in Chicago that provides free rosacea education, patient materials, physician resources, and research grants to rosacea patients and healthcare professionals, funded by donations and pharmaceutical educational grants.

What National Rosacea Society does

The National Rosacea Society (NRS) is a 501(c)(3) nonprofit patient-advocacy organization founded in 1992 and headquartered in Chicago, Illinois. Its mission is to improve outcomes for the estimated 16 million Americans and 415 million people worldwide affected by rosacea by raising disease awareness, providing free education, and funding medical research. The NRS primarily serves rosacea patients and a secondary audience of dermatologists, physicians, and eye-care specialists who rely on its clinical tools and patient handouts. With 1–10 employees, the organization operates a community-led model anchored by rosacea.org, the quarterly Rosacea Review newsletter, an annual April Rosacea Awareness Month campaign, and presence across Facebook, Instagram, Twitter, Pinterest, Bluesky, LinkedIn, and YouTube.

The NRS's core deliverables are content-based rather than technology-based. Its product set comprises patient education booklets (Understanding Rosacea, Coping with Rosacea, Managing Rosacea, Recognizing Redness, and the 2026-updated Rosacea Diary), the Seal of Acceptance certification program for rosacea-friendly skin care and cosmetics (currently covering 50+ products), the Rosacea Review newsletter (published since 1996), physician resources including clinical scorecards and treatment algorithms, and a Research Grants Program that has been funding rosacea research for 26 consecutive years. All materials are distributed free of charge via downloadable PDFs, email, postal mail, and bulk distribution to medical practices. No proprietary technology platform, mobile app, or AI/ML capability is offered.

The organization's funding model is dual-track. The first stream is individual donations and membership fees from patients and supporters. The second stream is unrestricted educational grants from pharmaceutical, dermatology, medical-device, and cosmetics companies — six of which are named for the 2026 website-maintenance cycle: Journey Medical, Mayne Pharma, Crescel, Sente Labs, Laura Geller, and Cutera. There are no shareholders, parent company, or venture capital involvement; governance is provided by a Board of Directors and a Medical Advisory Board, and leadership is exercised through a small editorial and program team including a Managing Editor, an Editor (who also serves as president of Dermatology and Skin Care Center of Birmingham), and a Social Media Editor.

National Rosacea Society firmographics

Firmographics
Name
National Rosacea Society
Legal name
National Rosacea Society
Website
https://rosacea.org
Company type
Private
Founded year
1992
Operating status
Operating
Headcount range
1–10 employees
Short description
The National Rosacea Society is a 501(c)(3) nonprofit founded in 1992 and headquartered in Chicago that provides free rosacea education, patient materials, physician resources, and research grants to rosacea patients and healthcare professionals, funded by donations and pharmaceutical educational grants.
Ownership category
akta.pro rank

National Rosacea Society industry classification

Industry
Product category
Patient Advocacy / Nonprofit Health Organization
NAICS
Professional Organizations (813920)
SIC
Services-Membership Organizations (8600)
akta.pro primary industry
Sensitive Skin & Rosacea-Calming Treatments (HSALADAF)

Keywords

  • Rosacea patient education
  • Medical research grants
  • Patient advocacy nonprofit
  • Skin condition awareness
  • Seal of acceptance certification

Where National Rosacea Society is headquartered

Location

Headquarters

HQ city
Chicago
HQ country
United States
HQ region
North America

Offices1 record

Markets served

National Rosacea Society business model

Business model
GTM type
B2C
Offering type
Services
Cost components
Personnel, Marketing or Sales, Operations, Others

Revenue model

  1. Donations and Membership: The organization collects individual donations and membership fees from patients and supporters to fund research grants and public education programs.
  2. Pharmaceutical Company Educational Grants: Website maintenance is supported by unrestricted educational grants from pharmaceutical and dermatology companies including Journey Medical, Mayne Pharma, Crescel, Sente Labs, Laura Geller, and Cutera.

Go-to-market motion1 record

Distribution channels3 records

Marketing channels5 records

National Rosacea Society product offering

Product offering

Core offering

The National Rosacea Society (NRS) is a 501(c)(3) nonprofit organization that provides free educational resources to rosacea patients, funds medical research into the cause and treatment of rosacea, and runs a Seal of Acceptance program that certifies skin care and cosmetic products deemed appropriate for sensitive rosacea-prone skin.

Product overview

The National Rosacea Society operates primarily as an educational and awareness organization rather than a technology product company. Its core offerings consist of patient education materials including the Rosacea Diary (updated 2026), Understanding Rosacea Brochure, Coping with Rosacea Brochure, Managing Rosacea Brochure, and Recognizing Redness Booklet. The society also runs a Seal of Acceptance Program that certifies skin care and cosmetic products as suitable for rosacea patients. Additionally, it publishes the Rosacea Review Newsletter and funds medical research through its Research Grants Program.

Differentiator

Problem solved

Functional benefit

Companies that use National Rosacea Society

Customer profile

Segments2 records

Ideal customer profiles4 records

National Rosacea Society technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

National Rosacea Society partnerships and signals

Strategic signal

Scale indicators6 records

Recent moves7 records

Expansion highlights5 records

National Rosacea Society competitors and assessment

Company assessment

Direct peers

  • Dermatology Foundation: Dermatology research funding nonprofit awarding grants to advance skin science. Direct peer on the research-grants vertical of NRS's mission, with similar donor and industry funding architecture.
  • National Eczema Association: Patient advocacy nonprofit for eczema, operating a near-identical model of patient education, physician resources, research grants, and disease-specific awareness campaigns. Direct structural and operational analogue to NRS.
  • Lupus Foundation of America: Chronic disease patient advocacy nonprofit with similar operational scale, pharma grant reliance, and member/donor-driven education model. Comparable build of patient resources, physician tools, and research programming.
  • Asthma and Allergy Foundation of America: Patient advocacy nonprofit for asthma and allergies with analogous chronic-condition awareness, education, research funding, and pharma sponsorship model. Comparable scale and operational footprint.
  • Skin Cancer Foundation: Skin disease advocacy nonprofit focused on awareness, education, and physician resources. Mirrors NRS's content-library, awareness-month, and physician outreach playbook in a different skin condition.
  • American Skin Association: Skin health advocacy nonprofit combining research funding and public education. Closely comparable mission, structure, and donor base to NRS, though broader across dermatologic conditions.
  • National Psoriasis Foundation: Patient advocacy nonprofit for psoriasis with patient education, support resources, research funding, and a comparable donor/pharma sponsorship model. Closest peer in scale and mission within dermatology.

Others

  • Society for Investigative Dermatology: Professional research society for dermatology investigators. Relevant adjacency for NRS's research grants program and scientific advisory operations, though it serves investigators rather than patients directly.
  • American Autoimmune Related Diseases Association: Umbrella advocacy organization for autoimmune diseases. Thematically adjacent to NRS as a chronic-condition advocacy model, useful for comparison on coalition-style fundraising and cross-disease awareness.

Broad incumbents

  • American Academy of Dermatology: Largest professional dermatology association in the US, with far broader physician engagement, CME, and patient education capabilities. Overlaps with NRS on rosacea physician resources but operates as a multi-disease umbrella.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks5 records

Key highlights6 records

Customer concentration

National Rosacea Society social profiles

Digital presence

National Rosacea Society financial estimates

Financial estimate

Revenue estimate

Valuation estimate

National Rosacea Society leadership team

Management profile

Number of profiles

Profiles3 records

National Rosacea Society funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

National Rosacea Society 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 National Rosacea Society

What does National Rosacea Society do?

The National Rosacea Society (NRS) is a 501(c)(3) nonprofit organization that provides free educational resources to rosacea patients, funds medical research into the cause and treatment of rosacea, and runs a Seal of Acceptance program that certifies skin care and cosmetic products deemed appropriate for sensitive rosacea-prone skin.

Is National Rosacea Society a public or private company?

National Rosacea Society is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was National Rosacea Society founded?

National Rosacea Society was founded in 1992. It employs 1 to 10 people.

Where is National Rosacea Society based?

National Rosacea Society is headquartered in Chicago, United States, in the North America region.

How does National Rosacea Society make money?

Two revenue lines are on record. Donations and Membership is the primary driver. The others are pharmaceutical Company Educational Grants.

Who are National Rosacea Society's main competitors?

Direct peers on record are Dermatology Foundation, National Eczema Association, Lupus Foundation of America, Asthma and Allergy Foundation of America, Skin Cancer Foundation, American Skin Association and National Psoriasis Foundation. Others are Society for Investigative Dermatology and American Autoimmune Related Diseases Association. American Academy of Dermatology is listed as a broad incumbent.

Does National Rosacea Society have an API?

No public API is recorded for National Rosacea Society.

What industry is National Rosacea Society in?

National Rosacea Society's product category is Patient Advocacy / Nonprofit Health Organization. Its primary akta.pro industry code is HSALADAF, Sensitive Skin & Rosacea-Calming Treatments. Its NAICS code is 813920 and its SIC code is 8600.

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