Mucus Relief Severe Cold Daytime Cold and Flu Nighttime
- Product NDC
- 36800-577
- 11-digit product format
- 368000577
- Labeler code
- 36800
- Product ID
- 36800-577_d0e85303-556a-3330-e053-2995a90ad924
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride
- Dosage form
- KIT
- Labeler
- TopCo Associates LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-07-31
- Marketing end
- 2021-11-30
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 36800-577-02 | 36800057702 | 1 KIT in 1 CARTON (36800-577-02) * 10 TABLET, COATED in 1 BLISTER PACK * 10 TABLET, COATED in 1 BLISTER PACK | 1 kit | 2017-07-31 | 0000-00-00 | No | No | Current |