Mucinex Sinus-Max Day Night
- Product NDC
- 63824-251
- 11-digit product format
- 638240251
- Labeler code
- 63824
- Product ID
- 63824-251_60cff976-38d2-4905-97df-059914815749
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride
- Dosage form
- KIT
- Labeler
- RB Health (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-11-20
- 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 |
|---|
| 63824-251-01 | 63824025101 | 1 KIT in 1 PACKAGE, COMBINATION (63824-251-01) * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2018-11-20 | 0000-00-00 | No | No | Current |