NDC product
Diphenhydramine HCl and Zinc Acetate
NDC 0363-0215 · Walgreen Company
Key facts
| Product NDC | 0363-0215 |
|---|---|
| Proprietary name | Diphenhydramine HCl and Zinc Acetate |
| Nonproprietary name | Extra Strength Itch Relief |
| Substances | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Dosage form | SPRAY |
| Route | TOPICAL |
| Labeler | Walgreen Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Jan 12, 2012 |
| 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: