Register entry
- Registered sites
- 0
- Active NDC listings
- 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 |
|---|---|
| gel | 1 |
| spray | 1 |
| Route | NDCs |
|---|---|
| cutaneous | 1 |
| topical | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| gold inti trade corporation | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| SKINTIFIC 3X ACID INTENSIVE ACNE TREATMENT | SALICYLIC ACID | gel, topical | 87467-002OTC MONOGRAPH DRUG |
| SKINTIFIC OUTDOOR SUN BROAD SPECTRUM SPF 50 | avobenzone, homosalate, octinoxate, octisalate, octocrylene, oxybenzone | spray, cutaneous | 87467-001OTC MONOGRAPH DRUG |
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Enquiry
Common questions
- Is Gold Inti Trade Corporation FDA approved?
- Gold Inti Trade Corporation 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 Gold Inti Trade Corporation make?
- 2 products are listed under Gold Inti Trade Corporation in the openFDA NDC Directory, most often as gel; spray. 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.