Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Labeller names
- 2
- 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 |
|---|---|
| lotion | 3 |
| Route | NDCs |
|---|---|
| topical | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| botanical science, inc. | 2 |
| botanical science technologies | 1 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ADVANCED PROTECTION SUNSCREEN SPF-30 | OCTINOXATE, OCTISALATE, ZINC OXIDE | lotion, topical | 70712-103OTC MONOGRAPH DRUG |
| MINERAL TINTED SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | lotion, topical | 70712-104OTC MONOGRAPH DRUG |
| WEIGHTLESS PROTECTION SPF 30 | OCTINOXATE, ZINC OXIDE, OCTISALATE | lotion, topical | 70712-102OTC MONOGRAPH DRUG |
Compare
Other companies listing octinoxate, octisalate, zinc oxide
- Likewise Incorporated0 sites · 4 NDC
Enquiry
Common questions
- Is Botanical Science Technologies FDA approved?
- Botanical Science Technologies 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 Botanical Science Technologies make?
- 3 products are listed under Botanical Science Technologies 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.