Mucus Relief
- Product NDC
- 55312-336
- 11-digit product format
- 553120336
- Labeler code
- 55312
- Product ID
- 55312-336_4cf10d75-94da-4ec4-b5db-ddab2a5fbd15
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Western Family Foods, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-01-31
- Marketing end
- 2021-12-30
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 20 mg/20mL; mg/20mL; mg/20mL; mg/20mL
- 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 |
|---|
| 55312-336-06 | 55312033606 | 177 mL in 1 BOTTLE, PLASTIC (55312-336-06) | 177 ml | 2015-01-31 | 2021-12-30 | No | No | Current |