United States · FDA National Drug Code directory
Arnicare Bruise
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
- 0220-9084_5a5bfbba-f7b9-6a0c-e063-6394a90a219d
- Product NDC
- 0220-9084
- Form
- GEL
- Composition / generic term
- ARNICA MONTANA
- Labeler
- Laboratoires Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20160201
- Source listing expiry
- 20271231
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 (0220-9084-54) / 45 g in 1 TUBE · 0220-9084-54
- 1 TUBE in 1 CARTON (0220-9084-59) / 75 g in 1 TUBE · 0220-9084-59
- 1 TUBE in 1 CARTON (0220-9084-66) / 120 g in 1 TUBE · 0220-9084-66
- 2 TUBE in 1 CARTON (0220-9084-85) / 120 g in 1 TUBE · 0220-9084-85
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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