NDC product
LIQUID · KAO USA
NDC 10596-194 · KAO USA
Key facts
| Product NDC | 10596-194 |
|---|---|
| Nonproprietary name | Octocrylene Ethylhexyl Salicylate Homosalate Butyl Methoxydibenzoylmethane |
| Substances | OCTISALATE, HOMOSALATE, OCTOCRYLENE, AVOBENZONE |
| Dosage form | LIQUID |
| Labeler | KAO USA |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| Marketing start | Dec 31, 2022 |
| 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: