Raqiyyah Pippins focuses her practice in the areas of FDA's regulation of food, dietary supplement, cosmetic, drug and medical-device products sold directly to consumers as well as FTC and state regulation of the marketing and sale of consumer products. Ms. Pippins represents companies that are engaged in the development, marketing, import and export of consumer products, including conventional food, dietary supplements, drugs, cosmetics, medical devices, apparel and appliances. She also represents consumer product companies in advertising challenges (including numerous challenges before the National Advertising Division (NAD) of the Advertising Self-Regulatory Council), and defends companies in investigations conducted by the FDA, FTC, and state agencies regarding product marketing practices.

Ms. Pippins has particular experience assisting companies develop promotional strategies that account for the federal and state regulations governing direct-to-consumer product promotion. Her experience includes advising consumer product companies on relevant federal and state laws and regulations governing health-related claims for conventional food, dietary supplements, cosmetics, and devices (including IoT implications), assisting FDA-regulated companies with product development, monograph compliance and Rx-to-OTC switches, and counseling companies regarding the development of clinical and sensory studies intended to substantiate advertising claims. She is a trusted advisor of trade organizations supporting manufacturers of FDA-regulated products regarding FTC and state standards that also impact the risk profile for companies' product portfolios and is regularly invited to work directly with clients' marketing and research and development teams to help identify marketing strategies that are consistent with the desired risk threshold for the company.


  • Manufacturers of FDA-regulated products regarding effective product promotion via diverse mediums (e.g., labeling, website, television networks, social media and platforms intended for handheld-devices) while accounting for FDA, FTC, NAD, state regulation and other risk considerations.
  • One of the largest US drugstore chains in coordinating the review of more than 600 generic brand labels, including an assessment of claim substantiation and compliance with federal labeling regulations.
  • Retailers and manufacturers of FDA regulated products regarding adverse event reporting requirements and managing voluntary recalls.
  • Leading confectionary company in managing international legal review of new front-of-pack labeling system intended for use in twenty-four countries.
  • Consumer packaged goods companies in developing novel marketing strategies for conventional food, dietary supplement, and cosmetic products including use of health-benefit, nutrient content, product composition (e.g., natural or organic), and performance claims.
  • Manufacturers of FDA-regulated products in effectively engaging stakeholders in trade associations to comment regarding proposed FDA rulemakings impacting safety and labeling regulations.
  • Manufacturer of market-leading OTC allergy products in successful development and implementation of multi-faceted marketing campaigns for product portfolio, including 1st in class Rx-to-OTC switched intranasal corticosteroid product.
  • FDA-regulated companies with responses to FTC and state AG inquiries regarding advertising practices, including claim substantiation and adequate use of disclosures in advertisements.
  • Global Fortune 500 companies in challenges before the National Advertising Division (NAD) of the Advertising Self-Regulatory Council including challenges related to comparative health-benefit claims and preference testing.
  • Pharmaceutical companies regarding FDA adverse event reporting requirements and related Privacy Act and Freedom of Information Act considerations.


FLAVA Food Law Panel
University of Virginia School of Law, Charlottesville, VA
Legal Implications of Current Trends in Claims
ACI Advertising Claims Substantiation Boot Camp, New York, NY
FDA is Getting Personal: Warning letters reiterate Agency priorities, target consumer reviews, and trigger consumer class actions
HAPPI Magazine
FDA's 21st Century Cures Act Guidance Documents Clarify the Landscape for Digital Health Innovation
OTC Marketing and Advertising
CHPA OTC Academy, OTC 101 Seminar, New Brunswick, NJ


The Network Journal
"Top 40 Under Forty Achievers" (2015)
Ebony Magazine
"Top 30 Under Thirty" (2006)


  • JD, University of Virginia School of Law, 2006
  • BA, Stanford University, 2003
  • District of Columbia
  • Virginia
  • DC Board of Directors, Boys & Girls Club of Greater Washington
  • Board of Directors, Capital Youth Empowerment Program
  • Member, National Bar Association: Commercial Law Section
  • Member, American Bar Association
  • Delta Sigma Theta Sorority, Inc., Federal City Alumnae Chapter
  • Past National Chair, National Black Law Students Association

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