NAD Recommends P&G Discontinue “2X Strength Per Caplet” Claim for Pepto Bismol Ultra, Following Challenge by GSK

New York, NY – Sept. 26, 2019 – The National Advertising Division has recommended that The Procter & Gamble Company discontinue its “2X Strength per ounce,” “2X Strength per caplet,” and “Ultra Coat” claims for Pepto Bismol Ultra, following a challenge by GlaxoSmithKline Consumer Healthcare, the maker of competing TUMS antacid products.  NAD did not, however, find any basis to recommend a name change for the Pepto Bismol Ultra product.

NAD is an investigative unit of the advertising industry’s system of self-regulation and is a division of the BBB NP’s self-regulatory and dispute resolution programs.

The claims at issue, appearing on packaging, in online advertising, and on third party retail websites, included:

Express claims:

  • “Pepto Bismol Ultra.”
  • “Ultra Strength relief for upset stomachs.”
  • “When you’re in need of ultra strength for your digestive upsets, this is your Pepto-Bismol.”

Implied claims:

  • Pepto Bismol has greater strength (i.e., delivers more of the active ingredient per dose) than regular Pepto Bismol.
  • Pepto Ultra has greater efficacy and/or provides greater relief than regular Pepto Bismol, specifically calling out its applicability in times of great need, i.e., “[w]hen you’re in need of ultra strength.”

Pepto Bismol Ultra (“Pepto Ultra”) is an OTC drug, available in liquid and caplet form, designed to treat various digestive conditions.  Pepto Ultra is marketed alongside the original version of Pepto Bismol (“Pepto Original”).  Both products contain the same amount of active ingredient – 525mg bismuth subsalicylate per dose – however, Pepto Ultra is delivered in a more concentrated strength form. Pepto Ultra and Pepto Original deliver the same strength per dose and are equally effective, but consumers are instructed to take a smaller dose of the more concentrated Pepto Ultra product. 

At issue before NAD was whether Pepto Ultra’s product name, packaging and other advertising communicate to consumers the misleading messages that Pepto Ultra has greater strength (i.e., more of the active ingredient per dose) or is more effective than Pepto Original.

The advertiser informed NAD in writing that it had permanently discontinued the claims “[u]ltra strength relief for upset stomachs,” and “[w]hen you’re in need of ultra strength for your digestive upsets, this is your Pepto-Bismol.”  NAD, relying on the advertiser’s representation that the claims have been permanently discontinued, did not review the claims on their merits.  However, the voluntarily discontinued claims will be treated, for compliance purposes, as though NAD recommended their discontinuance and the advertiser agreed to comply.

With regard to the Pepto Ultra product name standing alone, NAD found that “Ultra” by itself does not literally express, in a clear, specific or objectively provable way, that Pepto Ultra has greater strength per dose or greater symptom relief than Pepto Original.  Given the lack of extrinsic evidence of consumer confusion and absence of an expressly false claim, NAD determined that there was no basis to recommend a product name change. 

NAD recommended that the “2X Strength per ounce” and “2X Strength per caplet” claims be discontinued because they convey the unsupported message that Pepto Bismol Ultra has twice the strength per dose and is more effective than the original version of the product.  NAD noted that nothing in the four corners of the challenged advertising (i.e., the front of the product packaging) clearly and conspicuously informs consumers that “2X strength” means that Pepto Ultra is twice as concentrated as Pepto Original, thereby allowing consumers to take a smaller dose and receive the same symptom relief.

Finally, NAD recommended that P&G discontinue its “Ultra Coat” claim because it conveys the unsupported message that Pepto Bismol Ultra delivers increased or superior stomach coating as compared to the original product. Although P&G pointed to evidence that Pepto Ultra has increased viscosity as compared to Pepto Original, NAD determined that this data did not reliably demonstrate that a higher viscosity score translates into an increased or superior coating action that is meaningful to consumers.  In its advertiser’s statement, P&G stated that it “agrees to comply with NAD’s recommendations regarding advertising for its Pepto Ultra product.”

 

Subscribe to the Ad Law Insights or Privacy Initiatives newsletters for an exclusive monthly analysis and insider perspectives on the latest trends and case decisions in advertising law and data privacy.

 

 

 

 

Latest Decisions

Decision

Direct Selling Self-Regulatory Council Recommends Valentus Discontinue Earnings and Product Performance Claims

McLean, VA – December 23, 2024 – The Direct Selling Self-Regulatory Council (DSSRC) recommended Valentus, a direct selling company that sells nutritional and lifestyle products, discontinue earnings and health-related product performance claims made on social media and on the Valentus website.

Read the Decision Summary
Decision

Direct Selling Self-Regulatory Council Refers Olive Tree Earnings Claims to the FTC and California AG for Possible Enforcement Action

McLean, VA – December 20, 2024 – The Direct Selling Self-Regulatory Council (DSSRC) referred Olive Tree to the Federal Trade Commission (FTC) and California Attorney General's Office for possible enforcement action after Olive Tree failed to respond to a DSSRC inquiry into earnings claims.  

Read the Decision Summary
Decision

Children’s Advertising Review Unit Recommends JustPlay Discontinue or Modify Daisy the Yoga Goat Claims

New York, NY – December 19, 2024 - The Children’s Advertising Review Unit (CARU) launched an investigation into advertising for Just Play’s furReal Daisy the Yoga Goat seeking to determine if the toy’s product packaging and commercial advertisements comply with CARU’s Self-Regulatory Guidelines for Children’s Advertising.

Read the Decision Summary
Decision

In National Advertising Division Fast-Track SWIFT Challenge, Oral Essentials Voluntarily Modifies “Made in USA” Claims

New York, NY – December 19, 2024 – In a National Advertising Division challenge, Oral Essentials agreed to permanently modify its claim that certain Oral Essentials oral healthcare products are “Made in USA.” 

Read the Decision Summary