Mucinex Fast-Max
- Product NDC
- 63824-516
- 11-digit product format
- 638240516
- Labeler code
- 63824
- Product ID
- 63824-516_9a268e09-e2da-45c2-8b0e-9cb461405ee5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethrophan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride
- Dosage form
- KIT
- Labeler
- RB Health (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-12-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63824-516-01 | 63824051601 | 1 KIT in 1 PACKAGE, COMBINATION (63824-516-01) * 1 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON (63824-514-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2018-12-10 | 0000-00-00 | No | No | Current |