NDC product
Blistex Ivarest Poison Ivy Itch
NDC 10157-2100 · Blistex Inc.
Key facts
| Product NDC | 10157-2100 |
|---|---|
| Proprietary name | Blistex Ivarest Poison Ivy Itch |
| Nonproprietary name | Zinc Acetate and PRAMOXINE HYDROCHLORIDE |
| Substances | ZINC ACETATE, PRAMOXINE HYDROCHLORIDE |
| Dosage form | SPRAY |
| Route | TOPICAL |
| Labeler | Blistex Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M016 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| Marketing start | Feb 2, 2015 |
| 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: