Multi Symptom Cold Relief CF
- Product NDC
- 21130-382
- 11-digit product format
- 211300382
- Labeler code
- 21130
- Product ID
- 21130-382_550c8580-56b5-43cc-90a4-4998a44dcca5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin, Phenylephrine
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Safeway, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-06-30
- Marketing end
- 2022-12-30
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 20 mg/10mL; mg/10mL; mg/10mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-382-04 | 21130038204 | 1 BOTTLE, PLASTIC in 1 BOX (21130-382-04) > 118 mL in 1 BOTTLE, PLASTIC | 2014-06-30 | 2022-12-30 | No | No | Current |