NDC product
Anti Bacterial Hand Gel Honolulu Sun
NDC 62670-6751 · Bath & Body Works, Inc.
Key facts
| Product NDC | 62670-6751 |
|---|---|
| Proprietary name | Anti Bacterial Hand Gel |
| Nonproprietary name | Alcohol |
| Substances | ALCOHOL |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Bath & Body Works, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | Nov 18, 2024 |
| Marketing end | Nov 18, 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