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Data / Drug companies / Menthol and camphor

Menthol and camphor: 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).

Menthol and camphor 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 gel; liniment; ointment, and the newest product started marketing on March 2, 2026.

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Companies listing it
7
Products
9
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Topical, Percutaneous, Transdermal
Brand names
Richtofit Rapid Active Arthritis, Lung Choy Shung Pain Relief Liquid, Sore No More Warm Therapy, Professional Therapy MuscleCare Pro, Yulam Die Da Wan Hua Pain Relieving, Ultra Strength Zheng Gu Shui, Pain Relief Balm, GuruNanda Pain Relief
openFDA record search
api.fda.gov

Companies that list menthol and camphor

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Madison One Acme Inc3liniment; oilOver the counter monograph drugsJune 1, 2023
Active and Innovative Inc.1creamOver the counter monograph drugsMay 3, 2024
Alaina Healthcare Private Limited1ointmentOver the counter monograph drugsOctober 7, 2025
Guangxi Yulin Pharmaceutical Group Co LTD1linimentOver the counter monograph drugsApril 4, 2023
Gurunanda, LLC1ointmentOver the counter monograph drugsSeptember 1, 2025
Richtofit Limited Liability Company1gelOver the counter monograph drugsMarch 2, 2026
Sombra Cosmetics Inc.1gelOver the counter monograph drugsJune 13, 2016

Dosage forms

Dosage formProductsShare
Gel222.2%
Liniment222.2%
Ointment222.2%
Cream111.1%
Oil111.1%
Plaster111.1%

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.