Childrens Dimetapp Multi-Symptom Cold and Flu
- Product NDC
- 0031-2249
- 11-digit product format
- 000312249
- Labeler code
- 0031
- Product ID
- 0031-2249_1e5f973d-b229-40b3-afd3-f7559be20b70
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-01-01
- Marketing end
- 2022-09-30
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 320 mg/10mL; mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0031-2249-04 | 00031224904 | 1 BOTTLE in 1 CARTON (0031-2249-04) > 118 mL in 1 BOTTLE | 1 bottle | 2020-01-01 | 2022-09-30 | No | No | Current |