Register entry
- Registered sites
- 0
- Active NDC listings
- 2
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human otc drug. By marketing category: OTC MONOGRAPH DRUG 2.
| Dosage form | NDCs |
|---|---|
| lotion | 2 |
| Route | NDCs |
|---|---|
| topical | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| probetter usa inc. | 1 |
| probetter usa, inc. | 1 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Timesavvy Hybrid Sheer Sun Serum Broad Spectrum SPF 50 | HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE | lotion, topical | 85241-001OTC MONOGRAPH DRUG |
| Timesavvy Hybrid XL Cushion Sun Serum SPF 50 | HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE | lotion, topical | 85241-061OTC MONOGRAPH DRUG |
Compare
Other companies listing homosalate, octisalate, octocrylene, zinc oxide
- Sun Bum, LLC0 sites · 123 NDC
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.