Multi-Symptom Daytime Cold Rapid Release
- Product NDC
- 41163-560
- 11-digit product format
- 411630560
- Labeler code
- 41163
- Product ID
- 41163-560_a3b5b1f2-2362-4195-b6d6-2f6214bdac15
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- SUPERVALU INC.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2008-03-29
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 41163-560-08 | 41163056008 | 2 BLISTER PACK in 1 CARTON (41163-560-08) > 12 TABLET, COATED in 1 BLISTER PACK | 2 blister pack | 2008-03-29 | 0000-00-00 | No | No | Current |