NDC product
Extra Strength Itch Stopping
NDC 52000-071 · Universal Distribution Centre LLC
Key facts
| Product NDC | 52000-071 |
|---|---|
| Proprietary name | Extra Strength |
| Nonproprietary name | Itch Stopping Cream |
| Substances | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Universal Distribution Centre LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M016 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Jan 21, 2021 |
| 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: