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Data / Drug companies / Allantoin 0.5%

Allantoin 0.5%: 4 companies and 5 products in the FDA NDC directory

Allantoin 0.5% 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 gel, and the newest product started marketing on April 30, 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
Meijer Scar Gel, QC Scar, Rite Aid Scar, DCH Scar
openFDA record search
api.fda.gov

Companies that list allantoin 0.5%

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Meijer, Inc.2gelOver the counter monograph drugsApril 30, 2026
Chain Drug Marketing Association1gelOver the counter monograph drugsAugust 16, 2021
Derma Care Research Labs, LLC1gelOver the counter monograph drugsOctober 5, 2021
Rite Aid Corporation1gelOver the counter monograph drugsSeptember 15, 2022

Dosage forms

Dosage formProductsShare
Gel5100%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs5100%

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.