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Data / Drug companies / Octinoxate, octisalate, zinc oxide

Octinoxate, octisalate, zinc oxide: 6 companies and 11 products in the FDA NDC directory

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

Octinoxate, octisalate, zinc oxide is listed in the FDA National Drug Code Directory by 6 companies, with 11 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 March 4, 2025.

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Companies listing it
6
Products
11
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Meijer Kids Broad Spectrum SPF 50 Mineral Based Sunscreen, Likewise Hand Moisturizer - Sun Protectant SPF 50, Likewise Facial Moisturizer - Sun Protectant SPF 50 Normal To Dry Skin, Gold Mountain Beauty Collagen Broad Spectrum SPF 30, Botanical Soothing SPF-30, Control Corrective Intensive Skin Brightening SPF-30 Sunscreen, Likewise Facial Moisturizer - Sun Protectant SPF 50 Normal To Oily Skin, Coppertone Defend and Clear
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Companies that list octinoxate, octisalate, zinc oxide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Control Corrective Skincare Inc4creamOver the counter monograph drugsSeptember 11, 2018
Likewise Incorporated3creamOver the counter monograph drugsJune 20, 2011
Beiersdorf Inc1lotionOver the counter monograph drugsNovember 2, 2020
Botanical Science, Inc.1lotionOver the counter monograph drugsMarch 4, 2025
Meijer Distribution Inc1lotionOver the counter monograph drugsNovember 6, 2018
TT Fitness, Inc1creamOver the counter monograph drugsJune 10, 2020

Dosage forms

Dosage formProductsShare
Cream872.7%
Lotion327.3%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs11100%

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.