Rapid Release Pain Relief PM
- Product NDC
- 41250-556
- 11-digit product format
- 412500556
- Labeler code
- 41250
- Product ID
- 41250-556_d030ae2f-64d3-4ab1-8036-afed2c980566
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen and Diphenhydramine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2007-12-17
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record