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Data / Drug companies / Zinc oxide, octinoxate, and octisalate

Zinc oxide, octinoxate, and octisalate: 2 companies and 2 products in the FDA NDC directory

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

Zinc oxide, octinoxate, and octisalate is listed in the FDA National Drug Code Directory by 2 companies, with 2 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 spray; cream, and the newest product started marketing on March 4, 2020.

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Companies listing it
2
Products
2
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
BabyGanics Sunscreen 30 SPF, Touch Anti-Aging SPF 30 Moisturizer
openFDA record search
api.fda.gov

Companies that list zinc oxide, octinoxate, and octisalate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Diractions Capital LLC1creamOver the counter monograph drugsMarch 4, 2020
Kas Direct LLC DBA BabyGanics1sprayOver the counter monograph drugsJune 21, 2013

Dosage forms

Dosage formProductsShare
Spray150%
Cream150%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs2100%

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.