Register entry
- Registered sites
- 0
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 0
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ULTA FACE SPF 30 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE | lotion, topical | 62296-8292OTC MONOGRAPH NOT FINAL |
Compare
Other companies listing avobenzone, homosalate, octisalate, octocrylene, oxybenzone
- L'Oreal USA Products Inc5 sites · 213 NDC
- Fruit Of The Earth, Inc.2 sites · 37 NDC
- Laboratoires Clarins1 site · 14 NDC
- Aloe Care International, LLC0 sites · 18 NDC
Enquiry
Common questions
- Is Ulta FDA approved?
- Ulta holds no registered establishment of its own; 1 drug product is listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Ulta make?
- 1 product is listed under Ulta 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.