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Data / Drug companies / Zinc oxide 24%

Zinc oxide 24%: 4 companies and 5 products in the FDA NDC directory

Zinc oxide 24% is listed in the FDA National Drug Code Directory by 4 companies, with 5 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; lotion, and the newest product started marketing on May 5, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
4
Products
5
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Surface Sun SPF 50 Mineral Sunscreen, Onsart Mineral Sunscreen SPF 50, Eucerin Sensitive Mineral Face Sunscreen SPF 35, Onsart Mineral Sunscreen, Universkin By Alma Daily Mineral Serum Broad Spectrum SPF50
openFDA record search
api.fda.gov

Companies that list zinc oxide 24%

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Guangzhou Huixue Biotechnology Co., Ltd.2sprayOver the counter monograph drugsJanuary 27, 2026
Beiersdorf Inc1lotionOver the counter monograph drugsJanuary 1, 2023
Surface Products Corp1sprayOver the counter monograph drugsMay 5, 2026
Universkin1lotionOver the counter monograph drugsDecember 25, 2025

Dosage forms

Dosage formProductsShare
Spray360%
Lotion240%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs5100%

Pharmacologic classes

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