Bayer A+D Diaper Rash Cream Recall: Labeling Issue
Bayer recalls A+D Diaper Rash Cream with Dimethicone 1% and Zinc Oxide 10% due to labeling claims. Check UPCs and lot numbers for affected products.
Lower-risk recall
Labeling: Incorrect/Undeclared Excipients: Firm is recalling A+D Diaper Rash Cream due to a labeling claim issue.
Contact the company
What happened, in plain English
Bayer is recalling A+D Diaper Rash Cream products with specific UPCs and lot numbers because of a labeling issue. This recall does not involve safety risks but addresses incorrect labeling claims. Read more at govinfonow.com/recall/41927-bayer-a-d-diaper-rash-cream-recall-labeling-issue.
Source Summary by GovInfoNow · govinfonow.com/recall/41927-bayer-a-d-diaper-rash-cream-recall-labeling-issue · Updated October 8, 2026 · FDA enforcement record: FDA #D-0604-2017
Cite this page
“Bayer A+D Diaper Rash Cream Recall: Labeling Issue.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41927-bayer-a-d-diaper-rash-cream-recall-labeling-issue. Based on FDA recall #D-0604-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0604-2017%22&limit=1).
Why it’s dangerous
The product has incorrect or undeclared excipients listed on its label. This labeling issue means the product might not be as described, but it does not pose a direct health risk.
Who’s affected
Parents and caregivers of infants who use A+D Diaper Rash Cream. Infants using the recalled products are most at risk due to potential labeling confusion.
How to tell if you have this one
Check the UPC codes: 041100811288 (1.5 oz), 041100811301 (3 oz), or 041100811325 (4 oz). Also look for specific lot numbers and expiration dates listed in the recall notice.
- Brand
Bayer- Product
Bayer HealthCare Pharmaceuticals, Inc. recalls A+D Diaper Rash Cream with Dimethicone 1% and Zinc Oxide 10%, Packaged in a) 1.5 oz (42.5g) ( UPC 041100811288),…- Category
Drug
What to do — step by step
Check Product Details
Review the UPC code and lot number on the product to determine if it matches the recalled items listed in the notice.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwid, Puerto Rico, and Iceland” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product dangerous?
No, this recall is due to labeling issues, not a safety hazard. The product is safe to use but the labeling may be incorrect.
What should I do if I have this product?
Check the UPC and lot number against the recall list. If it matches, you do not need to stop using it but should contact Bayer for clarification.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0604-2017 (February 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0604-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.