United States · FDA National Drug Code directory
Arnicare
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
- 0220-9000_3a728515-f1d3-bcb9-e063-6294a90a4910
- Product NDC
- 0220-9000
- Form
- GEL
- Composition / generic term
- ARNICA MONTANA
- Labeler
- Laboratoires Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20070109
- Source listing expiry
- 20261231
Source-listed ingredients
- ARNICA MONTANA — 1 [hp_X]/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 PACKAGE (0220-9000-54) / 45 g in 1 TUBE · 0220-9000-54
- 1 TUBE in 1 PACKAGE (0220-9000-59) / 75 g in 1 TUBE · 0220-9000-59
- 1 TUBE in 1 PACKAGE (0220-9000-65) / 14 g in 1 TUBE · 0220-9000-65
- 1 TUBE in 1 PACKAGE (0220-9000-66) / 120 g in 1 TUBE · 0220-9000-66
- 1 TUBE in 1 PACKAGE (0220-9000-84) / 45 g in 1 TUBE · 0220-9000-84
- 2 TUBE in 1 PACKAGE (0220-9000-85) / 120 g in 1 TUBE · 0220-9000-85
- 2 TUBE in 1 PACKAGE (0220-9000-86) / 45 g in 1 TUBE · 0220-9000-86
- 5 g in 1 POUCH (0220-9000-94) · 0220-9000-94
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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