Arnica Montana 30C HPUS

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Arnica Montana 30C HPUS
Generic name
ARNICA MONTANA
Manufacturer
VITAMEDICA, INC.
Product type
HUMAN OTC DRUG
SPL set ID
d0d19cc4-6d45-467f-a032-bc249f6b7a1a
SPL ID
65a8e37b-4471-4633-b008-05a39cf45dfc
Version
1
Effective date
2026-03-12
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:45:56
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Ask a doctor before use if pregnant or breastfeeding. Stop use or consult a physician if • Any adverse reactions occur • Symptoms persist for more than 14-days or worsen Keep this and all medications out of reach of children. In case of an emergency or accidental overdose, contact a medical professional or Poison Control immediately. CONTAINS: Lactose (milk) • Do not use if seal is broken or shows any signs of tampering. • Store at 68-77°F (20-25°C)

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.