NDC product
SunPlus SPF 30 Everyday Inspired Broad Spectrum Sunscreen
NDC 84661-522 · SUNPLUS SKIN CARE LLC
Key facts
| Product NDC | 84661-522 |
|---|---|
| Proprietary name | SunPlus SPF 30 Everyday Inspired Broad Spectrum Sunscreen |
| Nonproprietary name | AVOBENZONE, OCTISALATE, OCTOCRYLENE |
| Substances | AVOBENZONE, OCTISALATE, OCTOCRYLENE |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | SUNPLUS SKIN CARE LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Aug 5, 2024 |
| 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: