Register entry

ProBetter USA, Inc.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
2
Labeller names
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
lotion2
RouteNDCs
topical2
Labeller name on the listingNDCs
probetter usa inc.1
probetter usa, inc.1
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
Timesavvy Hybrid Sheer Sun Serum Broad Spectrum SPF 50HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDElotion, topical85241-001OTC MONOGRAPH DRUG
Timesavvy Hybrid XL Cushion Sun Serum SPF 50HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDElotion, topical85241-061OTC MONOGRAPH DRUG
Compare

Other companies listing homosalate, octisalate, octocrylene, zinc oxide

Enquiry

Common questions

Is ProBetter USA, Inc. FDA approved?
ProBetter USA, Inc. 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 ProBetter USA, Inc. make?
2 products are listed under ProBetter USA, Inc. in the openFDA NDC Directory, most often as lotion. 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.