NDC product
Baby Butz
NDC 52358-0001 · Olen Skin Care Corporation
Key facts
| Product NDC | 52358-0001 |
|---|---|
| Proprietary name | Baby Butz |
| Nonproprietary name | Zinc Oxide |
| Substances | ZINC OXIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Olen Skin Care Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M016 |
| Marketing start | Jul 15, 2013 |
| Marketing end | Oct 1, 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