NDC product
Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light
NDC 10056-030 · Access Business Group LLC
Key facts
| Product NDC | 10056-030 |
|---|---|
| Proprietary name | Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light |
| Nonproprietary name | ENSULIZOLE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Substances | ENSULIZOLE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Access Business Group LLC |
| 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 | Dec 11, 2015 |
| 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: