United States · FDA National Drug Code directory
Arnica Montana
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 53499-3571_626305bd-4ae7-4180-a6b5-baf5db47c1e5
- Product NDC
- 53499-3571
- Form
- TABLET
- Composition / generic term
- Arnica Montana
- Labeler
- Schwabe North America, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20060101 / 20270331
Source-listed ingredients
- ARNICA MONTANA — 30 [hp_C]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, GLASS (53499-3571-2) · 53499-3571-2
- 250 TABLET in 1 BOTTLE, GLASS (53499-3571-3) · 53499-3571-3
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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