NDC product
Itch Relief
NDC 69842-235 · CVS Pharmacy
Key facts
| Product NDC | 69842-235 |
|---|---|
| Proprietary name | Itch Relief |
| Nonproprietary name | Diphenhydramine HCl and Zinc Acetate |
| Substances | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Dosage form | AEROSOL, SPRAY |
| Route | TOPICAL |
| Labeler | CVS Pharmacy |
| 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 | Feb 1, 2019 |
| Listing certified through | Dec 31, 2027 |
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: