Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human otc drug. By marketing category: OTC MONOGRAPH DRUG 3.
| Dosage form | NDCs |
|---|---|
| cream | 2 |
| gel | 1 |
| Route | NDCs |
|---|---|
| topical | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| omnilife usa, inc. | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| SEYTU Body Sunscreen | titanium dioxide and zinc oxide | cream, topical | 84271-001OTC MONOGRAPH DRUG |
| SEYTU Facial Sunscreen | titanium dioxide and zinc oxide | cream, topical | 84271-000OTC MONOGRAPH DRUG |
| SEYTU Spot | Salicylic Acid | gel, topical | 84271-002OTC MONOGRAPH DRUG |
Compare
Other companies listing titanium dioxide and zinc oxide
- L'Oreal USA Products Inc5 sites · 213 NDC
- Colorescience, Inc.1 site · 36 NDC
- Arbonne International, LLC1 site · 7 NDC
Enquiry
Common questions
- Is Omnilife USA, Inc. FDA approved?
- Omnilife USA, Inc. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Omnilife USA, Inc. make?
- 3 products are listed under Omnilife USA, Inc. in the openFDA NDC Directory, most often as cream; gel. 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.