Data / Drug companies / Zinc oxide sunscreen
Zinc oxide sunscreen: 5 companies and 59 products in the FDA NDC directory
Zinc oxide sunscreen is listed in the FDA National Drug Code Directory by 5 companies, with 59 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; spray, and the newest product started marketing on October 5, 2026.
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- Companies listing it
- 5
- Products
- 59
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Topical
- Brand names
- Reef Safe - Vitamin C Sunscreen SPF50, Zinc Five-0 Baby and Kids Mineral Sunscreen SPF50, Marie Originals - ProActive Sunscreen, Organic Sunscreen, AussieZinc Mineral Sunscreen Vegan and Organic Mozzie Repellant, Thermasun SPF50 Mineral Zinc Facial Sunscreen, Reefsun Sunscreen SPF50, Sun Zapper - Face Pure Zinc Sunscreen SPF30
- openFDA record search
- api.fda.gov
Companies that list zinc oxide sunscreen
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Veganic SKN Limited | 46 | cream | Over the counter monograph drugs | October 5, 2026 |
| Bentley Laboratories, LLC | 10 | lotion; cream | Over the counter monograph drugs | March 23, 2026 |
| CP Skin Health Group, Inc | 1 | spray | Over the counter monograph drugs | March 31, 2023 |
| Societe Clinical Skincare | 1 | cream | Over the counter monograph drugs | November 1, 2024 |
| Solara Suncare, Inc. | 1 | oil | Over the counter monograph drugs | July 24, 2024 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 48 | 81.4% |
| Lotion | 9 | 15.3% |
| Spray | 1 | 1.7% |
| Oil | 1 | 1.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 59 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Copper Absorption Inhibitor | 12 |
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.