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Data / Drug companies / Arnica montana

Arnica montana: 32 companies and 92 products in the FDA NDC directory

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

Arnica montana is listed in the FDA National Drug Code Directory by 32 companies, with 92 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 pellet; tablet; liquid, and the newest product started marketing on November 2, 2026.

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Companies listing it
32
Products
92
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral, Topical, Sublingual, Cutaneous
Brand names
Arnica, Arnica, Arnicare Bruise, Arnicare, Laboflex Arnipatch Muscle and Joint Patch, Arnica Bruise Cream, Arnica Recovery, Arnica 12C
openFDA record search
api.fda.gov

Companies that list arnica montana

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Boiron30pellet; tabletUnapproved homeopathic productsOctober 1, 2023
Hahnemann Laboratories, Inc.11pellet; capsuleUnapproved homeopathic productsMarch 12, 2021
Sevene USA6pelletUnapproved homeopathic productsMay 15, 2025
Vitamedica, Inc.6tabletUnapproved homeopathic productsMarch 12, 2026
Energique, Inc.3liquidUnapproved homeopathic productsAugust 11, 2015
Newton Laboratories, Inc.3liquidUnapproved homeopathic productsJanuary 28, 2026
BM Private Limited2globuleUnapproved homeopathic productsJanuary 1, 2015
Homeocare Laboratories2pellet; creamUnapproved homeopathic productsJune 11, 2012
Nartex Laboratorios Homeopaticos SA de CV2tablet; pelletUnapproved homeopathic productsMay 8, 2025
Natural Creations, Inc2liquidUnapproved homeopathic productsJuly 1, 2006
Rxhomeo Private Limited D.B.A. Rxhomeo, Inc2pellet; liquidUnapproved homeopathic productsMarch 19, 2024
Schwabe Mexico, S.A. de C.V.2tablet; gelUnapproved homeopathic productsJanuary 1, 2011
Schwabe North America, Inc.2gel; tabletUnapproved homeopathic productsJanuary 1, 2011
Beautivity LLC1creamUnapproved homeopathic productsMay 30, 2025
BioActive Nutritional, Inc.1liquidUnapproved homeopathic productsOctober 8, 2012
Dynamic Blending Specialists, Inc.1gelUnapproved homeopathic productsMarch 1, 2023
Eight and Company L.L.C1liquidUnapproved homeopathic productsMarch 8, 2019
Genuine Virgin Aloe Corporation1creamUnapproved homeopathic productsAugust 30, 2019
Huizhou Haosen Trading Co., Ltd.1creamUnapproved homeopathic productsSeptember 5, 2026
Jiashen International Trade Limited1creamUnapproved homeopathic productsMarch 14, 2026
Laboflex, Inc.1patchUnapproved homeopathic productsOctober 1, 2024
Laboratoire Schmidt-Nagel Inc.1globuleUnapproved homeopathic productsMay 1, 2025
Nantong Health & Beyond Hygienic Products Inc.1gelOver the counter monograph drugsJanuary 15, 2024
Ohm Pharma Inc.1pelletUnapproved homeopathic productsNovember 1, 2019
Professional Complementary Health Formulas1liquidUnapproved homeopathic productsAugust 15, 1984
Seroyal USA1creamUnapproved homeopathic productsJanuary 20, 2015
Shenzhen Fanyi Era Technology Co., Ltd1creamUnapproved homeopathic productsNovember 2, 2026
Sled Distribution, LLC1gelUnapproved homeopathic productsAugust 29, 2022
Standard Homeopathic Company1tabletUnapproved homeopathic productsFebruary 17, 1997
Total Operations Management LLC DBA:Bestmade Natural Products Micro1globuleUnapproved homeopathic productsJune 1, 2026
Walgreen Company1gelUnapproved homeopathic productsJune 20, 2019
Whole Foods Market, Inc.1gelUnapproved homeopathic productsSeptember 1, 2008

Dosage forms

Dosage formProductsShare
Pellet3639.1%
Tablet1415.2%
Liquid1213%
Cream1010.9%
Gel99.8%
Globule44.3%
Kit33.3%
Capsule22.2%
Patch11.1%
Ointment11.1%

Marketing categories

Marketing categoryProductsShare
Unapproved homeopathic products9198.9%
Over the counter monograph drugs11.1%

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.