United States · FDA National Drug Code directory
Arnica Power
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
- 61096-1032_1c3e7699-74cd-441a-92f3-d27b8267e8d9
- Product NDC
- 61096-1032
- Form
- LIQUID
- Composition / generic term
- Arnica montana
- Labeler
- Eight and Company L.L.C
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20190308
- Source listing expiry
- 20261231
Source-listed ingredients
- ARNICA MONTANA WHOLE — 3 [hp_X]/41mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, SPRAY in 1 CARTON (61096-1032-1) / 41 mL in 1 BOTTLE, SPRAY · 61096-1032-1
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 →