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Data / Drug companies / Camphor (synthetic), menthol

Camphor (synthetic), menthol: 5 companies and 7 products in the FDA NDC directory

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

Camphor (synthetic), menthol is listed in the FDA National Drug Code Directory by 5 companies, with 7 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; patch; solution, and the newest product started marketing on November 21, 2025.

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Companies listing it
5
Products
7
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical
Brand names
Neuroflex Topical Pain Relieving Liquid, Relieve and Relax Pain Relieving, Smooth Gator 60-Second Pain Relief, N-Labs Arcticzen Pain Relief Knee, Smooth Gator Foot and Leg Rub, Qntamax Muscle and Joint Pain Relieving, N-Labs ArcticZen Pain Relief Knee
openFDA record search
api.fda.gov

Companies that list camphor (synthetic), menthol

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Nutriomo Labs Pte. LTD2patchOver the counter monograph drugsNovember 21, 2025
Smooth Gator LLC2creamOver the counter monograph drugsJune 1, 2022
Almark Products Inc1solutionOver the counter monograph drugsApril 1, 2021
Mac Innovations, LLC1gelOver the counter monograph drugsJune 1, 2021
Qntamax LLC1ointmentOver the counter monograph drugsNovember 1, 2025

Dosage forms

Dosage formProductsShare
Cream228.6%
Patch228.6%
Solution114.3%
Gel114.3%
Ointment114.3%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs7100%

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.