Severe Cold and Flu
- Product NDC
- 69842-972
- 11-digit product format
- 698420972
- Labeler code
- 69842
- Product ID
- 69842-972_8cdfb5e5-19a2-4868-bdea-d16b0ceeab0c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS PHARMACY
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-08-08
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 69842-972-09 | 69842097209 | 2 BLISTER PACK in 1 PACKAGE (69842-972-09) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2019-08-08 | 0000-00-00 | No | No | Current |