basic care daytime
- Product NDC
- 72288-103
- 11-digit product format
- 722880103
- Labeler code
- 72288
- Product ID
- 72288-103_8722e3ee-189d-4632-b22a-0dc18632393c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Amazon.com Services LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-10-01
- 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
- 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 |
|---|
| 72288-103-62 | 72288010362 | 12 BLISTER PACK in 1 CARTON (72288-103-62) > 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 12 blister pack | 2020-10-01 | 0000-00-00 | No | No | Current |