NDC product
ONESSIP ADULT DAYTIME SEVERE COLD AND FLU
NDC 87078-972 · MEDWISE LIFESCIENCES INC.
Key facts
| Product NDC | 87078-972 |
|---|---|
| Proprietary name | ONESSIP ADULT DAYTIME SEVERE COLD AND FLU |
| Nonproprietary name | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI |
| Substances | PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, GUAIFENESIN |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | MEDWISE LIFESCIENCES INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA] and 3 more |
| Marketing start | Dec 15, 2025 |
| 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: