Data / Drug companies / Zinc oxide, titanium dioxide, octinoxate, octisalate
Zinc oxide, titanium dioxide, octinoxate, octisalate: 2 companies and 9 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Zinc oxide, titanium dioxide, octinoxate, octisalate is listed in the FDA National Drug Code Directory by 2 companies, with 9 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, and the newest product started marketing on February 3, 2024.
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- Companies listing it
- 2
- Products
- 9
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Topical
- Brand names
- Dr.Jart Premium Beauty Balm Fair-Light, Dr.Jart Premium Beauty Balm Medium-Tan, Dr.Jart Premium Beauty Balm Light Medium-Medium, Dr.Jart Premium Beauty Balm Deep Tan-Deep, Elroel Pang Pang Sun Cushion S7, Elroel Pang Pang Sun Cushion Plus
- openFDA record search
- api.fda.gov
Companies that list zinc oxide, titanium dioxide, octinoxate, octisalate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Have & Be Co., Ltd. | 7 | cream | Over the counter monograph drugs | August 11, 2023 |
| Monoglot Holdings Inc. | 2 | cream | Over the counter monograph drugs | February 3, 2024 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 9 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 9 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Copper Absorption Inhibitor | 6 |
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.