Skip to the page

Data / Drug companies / Wart remover gel

Wart remover gel: 4 companies and 4 products in the FDA NDC directory

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

Wart remover gel is listed in the FDA National Drug Code Directory by 4 companies, with 4 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 October 20, 2017.

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

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
4
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Salicylic Acid
openFDA record search
api.fda.gov

Companies that list wart remover gel

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
American Sales Company1gelOver the counter monograph drugsOctober 20, 2017
Premier Brands of America Inc.1gelOver the counter monograph drugsJanuary 1, 2013
Topco Associates LLC1gelOver the counter monograph drugsOctober 7, 2014
Walgreen Company1gelOver the counter monograph drugsAugust 24, 2012

Dosage forms

Dosage formProductsShare
Gel4100%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs4100%

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.