Daytime Severe Cold and Flu Relief Softgels
- Product NDC
- 49035-617
- 11-digit product format
- 490350617
- Labeler code
- 49035
- Product ID
- 49035-617_d20a1e8c-ea66-3bac-e053-2a95a90aacd6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOHPEN, DEXTROMETHORPHAN HBr, Guaifenesin, PHENYLEPHRINE HCl
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Wal-Mart Stores Inc
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-01-14
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49035-617-24 | 49035061724 | 2 BLISTER PACK in 1 CARTON (49035-617-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 2 blister pack | 2020-01-14 | 0000-00-00 | No | No | Current |