NDC product
Publix Maximum Strength
NDC 41415-715 · PUBLIX SUPER MARKETS, INC
Key facts
| Product NDC | 41415-715 |
|---|---|
| Proprietary name | Publix |
| Nonproprietary name | oxymetazoline hydrochloride |
| Substances | OXYMETAZOLINE HYDROCHLORIDE |
| Dosage form | SPRAY |
| Route | NASAL |
| Labeler | PUBLIX SUPER MARKETS, INC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC] |
| Marketing start | May 16, 2019 |
| 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: