Mucinex Fast-Max Cold, Flu and Sore Throat and Mucinex NightShift Cold and Flu
- Product NDC
- 63824-119
- 11-digit product format
- 638240119
- Labeler code
- 63824
- Product ID
- 63824-119_ed38f3a2-f3e3-36fe-e053-2995a90a5a8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride
- Dosage form
- KIT
- Labeler
- RB Health (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-07-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63824-119-66 | 63824011966 | 1 KIT in 1 CARTON (63824-119-66) * 180 mL in 1 BOTTLE (63824-503-66) * 180 mL in 1 BOTTLE (63824-015-66) | 1 kit | 2022-06-30 | 0000-00-00 | No | No | Current |