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Data / Drug companies / Homosalate, octisalate, and zinc oxide

Homosalate, octisalate, and zinc oxide: 2 companies and 8 products in the FDA NDC directory

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

Homosalate, octisalate, and zinc oxide is listed in the FDA National Drug Code Directory by 2 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 kit; cream; lotion, and the newest product started marketing on March 20, 2023.

The request: Get every company that lists homosalate, octisalate, and zinc oxide in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
2
Products
8
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
JLo Beauty That Big Screen Broad Spectrum SPF 30 Moisturizer, Sun Shield Broad Spectrum SPF 50 Matte Sunscreen, Obagi Medical Back To Basics (Including Obagi Medical Professional-C Serum 20), Obagi Skintrinsiq Brightening Protocol, Obagi Medical Back To Basics (Including Obagi Medical Professional-C Serum 15), Obagi Medical Way To Glow Kit, Obagi Nu-Derm FX System Normal - Dry Skin Transformation Complexion Brightening System, Obagi Nu-Derm FX System Normal - Oily Skin Transformation Complexion Brightening System
openFDA record search
api.fda.gov

Companies that list homosalate, octisalate, and zinc oxide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Obagi Cosmeceuticals LLC7kit; lotionOver the counter monograph drugsMarch 20, 2023
Ascendant Beauty LLC1creamOver the counter monograph drugsApril 1, 2021

Dosage forms

Dosage formProductsShare
Kit675%
Cream112.5%
Lotion112.5%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs675%
Other unapproved drugs225%

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.