Data / Drug companies / Sunscreen spf 50
Sunscreen spf 50: 6 companies and 10 products in the FDA NDC directory
Sunscreen spf 50 is listed in the FDA National Drug Code Directory by 6 companies, with 10 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are cream; lotion; aerosol, spray, and the newest product started marketing on September 23, 2026.
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- Companies listing it
- 6
- Products
- 10
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Topical, Cutaneous, Extracorporeal
- Brand names
- Zinc Oxide 20%, Ganrek Sunscreen Sprayer Broad Spectrum SPF 50, Zinc Oxide 14.69%, HydroGlow Daily Sunscreen Broad Spectrum SPF 50 Uva and Uvb
- openFDA record search
- api.fda.gov
Companies that list sunscreen spf 50
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Guangzhou Ariel Biotech Co., Ltd. | 3 | cream | Over the counter monograph drugs | March 25, 2026 |
| Ol Pharma Tech, LLC Drs Pharmacy | 3 | cream; lotion | Over the counter monograph drugs | January 1, 2024 |
| Dune Suncare, Inc. | 1 | stick | Over the counter monograph drugs | September 23, 2026 |
| Guangzhou Meixi Biotechnology Co., Ltd. | 1 | aerosol, spray | Over the counter monograph drugs | February 7, 2026 |
| IHerb, LLC | 1 | lotion | Over the counter monograph drugs | October 1, 2025 |
| The Soleil Group, LLC | 1 | lotion | Over the counter monograph drugs | October 9, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 5 | 50% |
| Lotion | 3 | 30% |
| Aerosol, spray | 1 | 10% |
| Stick | 1 | 10% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 10 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Copper Absorption Inhibitor | 2 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.