Register entry

SKINFINITY

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Registered sites
0
Active NDC listings
2
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 human otc drug. By marketing category: OTC MONOGRAPH DRUG 2.

Dosage formNDCs
cream2
RouteNDCs
topical2
Labeller name on the listingNDCs
skinfinity2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
ULTAMATTE PROTECTION SUNSCREENTitanium Dioxide, Zinc Oxidecream, topical85564-203OTC MONOGRAPH DRUG
ULTRA SILK PROTECTION SUNSCREENZinc Oxidecream, topical85564-208OTC MONOGRAPH DRUG
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Other companies listing titanium dioxide, zinc oxide

Enquiry

Common questions

Is SKINFINITY FDA approved?
SKINFINITY holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does SKINFINITY make?
2 products are listed under SKINFINITY in the openFDA NDC Directory, most often as cream. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.