NDC product
JACKET SPF-50 Broad Spectrum Sunscreen
NDC 71070-868 · BALSHI MD DERMACEUTICALS
Key facts
| Product NDC | 71070-868 |
|---|---|
| Proprietary name | JACKET SPF-50 Broad Spectrum Sunscreen |
| Nonproprietary name | ZINC OXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
| Substances | ZINC OXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | BALSHI MD DERMACEUTICALS |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| Marketing start | Apr 15, 2019 |
| 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: