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 |
|---|---|
| gel | 2 |
| liquid | 1 |
| Route | NDCs |
|---|---|
| topical | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| summer gelee llc | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| SUMMER GELEE SPF-30 | HOMOSALATE, OCTISALATE, OCTOCRYLENE | gel, topical | 84281-477OTC MONOGRAPH DRUG |
| SUMMER GELEE SPF-4 | HOMOSALATE, OCTISALATE | gel, topical | 84281-476OTC MONOGRAPH DRUG |
| Summer Face Sunscreen SPF 50 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | liquid, topical | 84281-893OTC MONOGRAPH DRUG |
Compare
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Enquiry
Common questions
- Is SUMMER GELEE LLC FDA approved?
- SUMMER GELEE LLC 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 SUMMER GELEE LLC make?
- 3 products are listed under SUMMER GELEE LLC in the openFDA NDC Directory, most often as gel; liquid. 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.