NDC product
Maximum Strength Mucus Relief Cold,Flu and Sore Throat
NDC 41163-737 · SUPERVALU INC
Key facts
| Product NDC | 41163-737 |
|---|---|
| Proprietary name | Maximum Strength Mucus Relief Cold,Flu and Sore Throat |
| Nonproprietary name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL |
| Substances | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | SUPERVALU INC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part341 |
| 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] |
| Marketing start | Sep 7, 2017 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: