NDC product
Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50
NDC 79265-8758 · Babo Botanicals, Inc.
Key facts
| Product NDC | 79265-8758 |
|---|---|
| Proprietary name | Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50 |
| Nonproprietary name | Zinc Oxide |
| Substances | ZINC OXIDE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | Babo Botanicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Oct 26, 2023 |
| 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: