Register entry
- Registered sites
- 1
- Active NDC listings
- 29
- Labeller names
- 2
- Live patents
- 0
- Countries
- 1
- Base
- United States
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| spa de soleil | 10443 Arminta Street, Sun Valley, California (CA) 91352, United States (USA) | Finished drug manufacture | 3003876848874682867 |
Catalogue
Drug listings by form and route
2929 active NDC listings: 29 human otc drug. By marketing category: OTC MONOGRAPH DRUG 29.
| Dosage form | NDCs |
|---|---|
| lotion | 9 |
| liquid | 6 |
| gel | 4 |
| cream | 3 |
| spray | 3 |
| solution | 2 |
| stick | 2 |
| Route | NDCs |
|---|---|
| topical | 29 |
| Labeller name on the listing | NDCs |
|---|---|
| spa de soleil | 27 |
| spa de soleil | 2 |
Catalogue
Marketed products
29| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Acne Care Lotn | salicylic acid | lotion, topical | 68062-2267OTC MONOGRAPH DRUG |
| Acne Cleanser | salicylic acid | liquid, topical | 68062-9905OTC MONOGRAPH DRUG |
| Acne Drying | salicylic acid | lotion, topical | 68062-9003OTC MONOGRAPH DRUG |
| Acne Moisturizer | salicylic acid | cream, topical | 68062-9907OTC MONOGRAPH DRUG |
| Acne Scrub | salicylic acid | liquid, topical | 68062-2257OTC MONOGRAPH DRUG |
| Acne Treatment Pads | salicylic acid | lotion, topical | 68062-9004OTC MONOGRAPH DRUG |
| BROTEGE Good Boy Protection SPF 15 and Retinol Daily Moisturizer | benzophenone-3, butyle methoxydibenzoylmethane, ethylhexyl salicylate, octocrylene | cream, topical | 68062-9981OTC MONOGRAPH DRUG |
| Dermatouch Acnecare Cleanser | salicylic acid | liquid, topical | 68062-9005OTC MONOGRAPH DRUG |
| Dermatouch Acnecare Facial Scrub | salicylic acid | liquid, topical | 68062-2255OTC MONOGRAPH DRUG |
| Dermatouch Acnecare Moisturizer | salicylic acid | cream, topical | 68062-9006OTC MONOGRAPH DRUG |
| Dermatouch Acnecare Pads | salicylic acid | liquid, topical | 68062-2256OTC MONOGRAPH DRUG |
| Dr Lift Advanced Antibacterial Wipes | Benzalkonium Chloride | liquid, topical | 68062-2244OTC MONOGRAPH DRUG |
| Dr Lift Antibacterial | Benzalkonium Chloride | lotion, topical | 68062-2243OTC MONOGRAPH DRUG |
| Dr Lift Antibacterial Body Scrub | benzalkonium chloride | gel, topical | 68062-2240OTC MONOGRAPH DRUG |
| Dr Lift Antibacterial Body Wash | benzalkonium chloride | gel, topical | 68062-2241OTC MONOGRAPH DRUG |
| Dr Lift Antibacterial Hand Sanitizer | ethyl alcohol | gel, topical | 68062-2250OTC MONOGRAPH DRUG |
| Dr Lift Antibacterial Hand Wash | benzalkonium chloride | gel, topical | 68062-2242OTC MONOGRAPH DRUG |
| Dr Lift Mineral SPF 30 | titanium dioxide | spray, topical | 68062-8312OTC MONOGRAPH DRUG |
| Dr Lift Mineral SPF 50 | titanium dioxide, zinc oxide | spray, topical | 68062-8311OTC MONOGRAPH DRUG |
| Dr Lift SPF 50 Clear Stick | Avobenzone, Homosalate, Octisalate, Octocrylene | stick, topical | 68062-8313OTC MONOGRAPH DRUG |
| Dr Lift SPF 50 Mineral Sunscreen Stick | Zinc Oxide | stick, topical | 68062-8314OTC MONOGRAPH DRUG |
| Mine Line Coconut Sunscreen SPF 50 | zinc oxide | lotion, topical | 68062-7301OTC MONOGRAPH DRUG |
| Moisture Sunscreen SPF 50 | titanium dioxide, zinc oxide | lotion, topical | 68062-9001OTC MONOGRAPH DRUG |
| Natural SPF 30 | titanium dioxide, zinc oxide | lotion, topical | 68062-8304OTC MONOGRAPH DRUG |
| Natural SPF 50 | titanium dioxide, zinc oxide | lotion, topical | 68062-8307OTC MONOGRAPH DRUG |
| Skin Relief Cream | hydrocortisone | lotion, topical | 68062-2266OTC MONOGRAPH DRUG |
| Tru Skin Rituals SPF 25 | titanium dioxide, zinc oxide | spray, topical | 68062-8801OTC MONOGRAPH DRUG |
| Vita Vie Antibacterial Wash | benzalkonium chloride | solution, topical | 68062-2217OTC MONOGRAPH DRUG |
| VitaVie | benzalkonium chloride | solution, topical | 68062-2219OTC MONOGRAPH DRUG |
Compare
Comparable companies in United States
- Hahnemann Laboratories, Inc. dba Alpine Pharmaceuticals1 site · 4,853 NDC
- NuCare Pharmaceuticals,Inc.1 site · 1,393 NDC
- Greer Laboratories, Inc.1 site · 1,328 NDC
- ASCLEMED USA INC. DBA ENOVACHEM1 site · 789 NDC
- Golden State Medical Supply Inc.1 site · 670 NDC
- Rising Pharma Holdings, Inc.1 site · 532 NDC
- HF Acquisition Co LLC1 site · 363 NDC
- ANI Pharmaceuticals, Inc.1 site · 299 NDC
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1 site · 273 NDC
- Newton Laboratories, Inc.1 site · 271 NDC
Enquiry
Common questions
- Is spa de soleil FDA approved?
- spa de soleil holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are spa de soleil's drugs manufactured?
- The FDA register lists Sun Valley, CA. Registered operations: finished drug manufacture.
- What drugs does spa de soleil make?
- 29 products are listed under spa de soleil in the openFDA NDC Directory, most often as lotion; liquid; 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.