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Data / Drug companies / Octisalate, octocrylene, zinc oxide

Octisalate, octocrylene, zinc oxide: 6 companies and 8 products in the FDA NDC directory

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

Octisalate, octocrylene, zinc oxide is listed in the FDA National Drug Code Directory by 6 companies, with 8 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, and the newest product started marketing on April 1, 2026.

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Companies listing it
6
Products
8
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Abib Dewy Tinted Sunscreen Glow Tube Deep, Abib Dewy Tinted Sunscreen Glow Tube Medium, Shiseido Ultimate Sun Protector, Sun Bum Signature Clear High Performance Sunscreen Broad Spectrum SPF 50 1.5 Oz, Abib Dewy Tinted Sunscreen Glow Tube Light, Sunstation Sport Sunscreen SPF 30, Sun Veil IlluminatingElixir Face Sunscreen SPF 38, Shade SPF30 Climate Control
openFDA record search
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Companies that list octisalate, octocrylene, zinc oxide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Fourcompany Co., LTD.3creamOver the counter monograph drugsApril 1, 2026
Impact Melanoma Inc1creamOver the counter monograph drugsMarch 19, 2025
Koco Life LLC1lotionOver the counter monograph drugsJanuary 15, 2026
Micro Current Technology, Inc.1creamOver the counter monograph drugsJune 1, 2025
Shiseido Americas Corporation1creamOver the counter monograph drugsMarch 1, 2025
Sun Bum, LLC1lotionOver the counter monograph drugsJanuary 1, 2025

Dosage forms

Dosage formProductsShare
Cream675%
Lotion225%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs8100%

Pharmacologic classes

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.