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Data / Drug companies / Octinoxate, titanium dioxide, and zinc oxide

Octinoxate, titanium dioxide, and zinc oxide: 4 companies and 26 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Octinoxate, titanium dioxide, and zinc oxide is listed in the FDA National Drug Code Directory by 4 companies, with 26 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 lotion; liquid, and the newest product started marketing on September 1, 2026.

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Companies listing it
4
Products
26
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Hera Black Cushion Foundation 22N1, Hera Black Cushion Foundation 21C2, Amorepacific Color Control Cushion Compact No.106, Amorepacific Color Control Cushion Compact No.208, Even Better Glow Light Reflecting Makeup Broad Spectrum SPF 15, Hera Black Cushion Foundation 13N1, Hera Black Cushion Foundation 17C2, Hera Black Cushion Foundation 21W1
openFDA record search
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Companies that list octinoxate, titanium dioxide, and zinc oxide

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Amorepacific Corporation20lotionOver the counter monograph drugsSeptember 1, 2026
Clinique Laboratories LLC4lotion; liquidOver the counter monograph drugsJune 25, 2020
Bobbi Brown Professional Cosmetics Inc.1liquidOver the counter monograph drugsJanuary 27, 2021
Makeup Art Cosmetics1liquidOver the counter monograph drugsAugust 1, 2015

Dosage forms

Dosage formProductsShare
Lotion2388.5%
Liquid311.5%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs26100%

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.