NDC product
Robitussin Medi-Soothers
NDC 0031-9306 · Haleon US Holdings LLC
Key facts
| Product NDC | 0031-9306 |
|---|---|
| Proprietary name | Robitussin Medi-Soothers |
| Nonproprietary name | dextromethorphan hydrobromide, menthol |
| Substances | DEXTROMETHORPHAN HYDROBROMIDE, MENTHOL, UNSPECIFIED FORM |
| Dosage form | LOZENGE |
| Route | ORAL |
| Labeler | Haleon US Holdings LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
| Marketing start | Jun 1, 2023 |
| 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: