NDC product
HDX
NDC 63148-100 · Apollo Health and Beauty Care
Key facts
| Product NDC | 63148-100 |
|---|---|
| Proprietary name | HDX |
| Nonproprietary name | Ethyl Alcohol |
| Substances | ALCOHOL |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Apollo Health and Beauty Care |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | Mar 22, 2021 |
| Marketing end | Jul 7, 2028 |
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