Mucus Relief Severe Congestion and Cough
- Product NDC
- 11822-3370
- Requested package NDC
- 11822-3370-9
- 11-digit product format
- 118223370
- Labeler code
- 11822
- Product ID
- 11822-3370_809a554d-5eba-4ddb-917a-551f6288d884
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-05-31
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 20 mg/20mL; mg/20mL; mg/20mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-3370 | MUCUS RELIEF SEVERE CONGESTION AND COUGH MAXIMUM STRENGTH (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [RITE AID CORPORATION] | 4 | Legacy NDC | 20240509_e85bbc70-c7f8-455d-8c0f-0c3c4ce8d5ac.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-3370-9 | 11822337009 | 266 mL in 1 BOTTLE, PLASTIC (11822-3370-9) | 266 ml | 2019-05-31 | 0000-00-00 | No | No | Current |