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Data / Drug companies / Homosalate, octisalate, avobenzone, octocrylene

Homosalate, octisalate, avobenzone, octocrylene: 7 companies and 9 products in the FDA NDC directory

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

Homosalate, octisalate, avobenzone, octocrylene is listed in the FDA National Drug Code Directory by 7 companies, with 9 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; liquid; gel, and the newest product started marketing on June 28, 2024.

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Companies listing it
7
Products
9
Generic (ANDA) products
0 (0.0%)
Application numbers
2
Routes
Topical
Brand names
Beauty 360 Accelerated Wrinkle Repair Moisturizer, Invisible Sunscreen SPF 40, Herbal Uv Defense SPF40, Cellular Laboratories De-Aging Sunscreen Broad Spectrum SPF 50 Plus, 3lab Perfect Sunscreen SPF 50 Plus Broad Spectrum, 3lab WW Day SPF40 Broad Spectrum, Nia 24 SPF 30
openFDA record search
api.fda.gov

Companies that list homosalate, octisalate, avobenzone, octocrylene

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
3lab, Inc2creamOver the counter monograph drugsMay 27, 2016
Cosmax USA, Corporation2gel; creamOver the counter monograph drugsJune 28, 2024
Amcol Health & Beauty Solutions, Inc. DBA1liquidOver the counter monograph drugsApril 1, 2016
CVS Pharmacy1liquidOver the counter monograph drugsApril 1, 2017
Market America1creamOver the counter monograph drugsMay 3, 2011
Niadyne Inc1lotionOver the counter monograph drugsJune 9, 2011
Particle Aesthetic Science LTD1creamOver the counter monograph drugsJune 28, 2024

Dosage forms

Dosage formProductsShare
Cream555.6%
Liquid222.2%
Gel111.1%
Lotion111.1%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs9100%

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.