CHILDRENS DIMETAPP NIGHTTIME COLD AND CONGESTION
- Product NDC
- 0031-2247
- 11-digit product format
- 000312247
- Labeler code
- 0031
- Product ID
- 0031-2247_8c3de1e3-e4d6-46d1-aa5b-783c3ecf89f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine hcl, phenylephrine hcl
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2007-11-01
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 6 mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0031-2247-13 | 00031224713 | 1 BOTTLE in 1 CARTON (0031-2247-13) > 118 mL in 1 BOTTLE | 1 bottle | 2007-11-01 | 0000-00-00 | No | No | Current |