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
0220-9021_5242ebff-163f-ebd4-e063-6294a90a61df
Product NDC
0220-9021
Form
CREAM
Composition / generic term
ARNICA MONTANA
Labeler
Laboratoires Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20070301
Source listing expiry
20271231

Source-listed ingredients

  • ARNICA MONTANA — 1 [hp_X]/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 40 g in 1 TUBE (0220-9021-60) · 0220-9021-60
  • 70 g in 1 TUBE (0220-9021-63) · 0220-9021-63
  • 1 TUBE in 1 BOX (0220-9021-68) / 14 g in 1 TUBE · 0220-9021-68
  • 1 TUBE in 1 BOX (0220-9021-82) / 120 g in 1 TUBE · 0220-9021-82
  • 2 TUBE in 1 BOX (0220-9021-88) / 120 g in 1 TUBE · 0220-9021-88

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →