Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu
- Product NDC
- 63824-557
- 11-digit product format
- 638240557
- Labeler code
- 63824
- Product ID
- 63824-557_a2cba0cd-fc98-49e6-a0c4-2b8a20fbcae9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride
- Dosage form
- KIT
- Labeler
- Reckitt Benckiser LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-08-25
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#