The U.S. Food and Drug Administration (FDA) just issued a warning to consumers about the potentially serious side effects of mistakenly swallowing <"https://www.yourlawyer.com/practice_areas/defective_drugs">Benadryl Extra Strength Itch Stopping Gel, an over-the-counter (OTC) product that should only be used on the skin. The FDA has received reports of serious side effects in people who mistakenly swallowed the product.
Some OTC Benadryl products are intended to be swallowed; however, Benadryl Extra Strength Itch Stopping Gel is only safe and effective when usedâ€”as directedâ€”on the skin. People swallowing the gel can ingest a dangerous amount of the active ingredient, diphenhydramine. Large doses of diphenhydramine can result in serious side effects such as unconsciousness, hallucinations, and confusion.
â€œConsumer confusion and incorrect product use are serious public health issues,” said Carol Holquist, R.Ph., director of FDAâ€™s Division of Medication Error Prevention and Analysis. â€œFDA is advising consumers and pharmacies to store products for the skin separately from products that should be swallowed.â€
Many pharmacies and grocery stores sell diphenhydramine topical gels that appear very similar in packaging to Benadryl Extra Strength Itch Stopping Gel. It is important that consumers also avoid swallowing these products.
To help consumers recognize that Benadryl Extra Strength Itch Stopping Gel is meant for use on the skin, the manufacturer, Johnson and Johnson, has taken the following actions:
â€¢ Changed the product label to add a new, prominent statement: â€œFor Skin Use Only.â€
â€¢ Attached a sticker to the cap of the product that says: â€œFor Skin Use Only.â€
â€¢ Initiated consumer studies to better understand factors that may contribute to consumers mistakenly swallowing Benadryl Extra Strength Itch Stopping Gel.
The FDA encourages manufacturers of similar products to adopt similar changes to their labeling and packaging.
Be aware that the repackaged product is currently stocked in retail stores. The FDA reminds consumers and health care professionals to always read the â€œDrug Factsâ€ box to identify active ingredients, directions for use, and warnings before using any OTC drug product.
Consumers and health care professionals are encouraged to report adverse side effects to the FDA’s MedWatch Adverse Event Reporting program at www.fda.gov/MedWatch or by calling 800-332-1088, toll-free.