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Data / Drug companies / Mineral sunscreen

Mineral sunscreen: 8 companies and 12 products in the FDA NDC directory

Mineral sunscreen is listed in the FDA National Drug Code Directory by 8 companies, with 12 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; stick; spray, and the newest product started marketing on August 20, 2026.

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Companies listing it
8
Products
12
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical, Cutaneous
Brand names
Babo SPF 30 Clear Zinc Fragrance Free Sport, Babo SPF 30 Clear Zinc Fragrance Free, doTERRA Sun Body, Babies Kidssun Protection, Babo Botanicals SPF 30 Daily Sheer Tinted Sunscreen - Natural Glow
openFDA record search
api.fda.gov

Companies that list mineral sunscreen

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Babo Botanicals, Inc.4stick; lotionOver the counter monograph drugsNovember 1, 2020
doTERRA International, LLC2spray; stickOver the counter monograph drugsAugust 12, 2026
Alaina Healthcare Private Limited1lotionOver the counter monograph drugsJune 12, 2026
Guangzhou Origin Beauty Cosmetics Co., Ltd.1lotionOver the counter monograph drugsAugust 20, 2026
Kayura Effect LLC1lotionOver the counter monograph drugsJune 12, 2026
Panergytek USA Inc1powderOver the counter monograph drugsJuly 20, 2025
The Center Brands, LLC1creamOver the counter monograph drugsSeptember 21, 2023
Trilogy Natural Products Limited1lotionOver the counter monograph drugsNovember 1, 2023

Dosage forms

Dosage formProductsShare
Lotion650%
Stick325%
Spray18.3%
Cream18.3%
Powder18.3%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs12100%

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.