United States · FDA National Drug Code directory
Arnicare Arnica
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
- 0220-9059_30d0f65b-a256-29b9-e063-6394a90a9b0f
- Product NDC
- 0220-9059
- Form
- TABLET
- Composition / generic term
- ARNICA MONTANA
- Labeler
- Laboratoires Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20110711
- Source listing expiry
- 20261231
Source-listed ingredients
- ARNICA MONTANA — 9 [hp_C]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET in 1 BLISTER PACK (0220-9059-04) · 0220-9059-04
- 120 TABLET in 1 BLISTER PACK (0220-9059-29) · 0220-9059-29
- 100 TABLET in 1 BLISTER PACK (0220-9059-92) · 0220-9059-92
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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