CVS Arnica

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
CVS Arnica
Generic name
ARNICA MONTANA FLOWER
Manufacturer
Natural Essentials, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
e49ae317-a03d-4576-ba27-f661469584ed
SPL ID
23706409-4128-bd90-e063-6394a90a1ee8
Version
2
Effective date
2024-10-01
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:24:42
Harmonized routes table
Harmonized routes
TOPICAL

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 For external use only When using this product Use only as directed do not use with other topical products. do not bandage tightly or use a heating pad. Stop use and ask a doctor If a rash or other adverse reaction occurs. symptoms worsen or persist for more than 7 days. avoid contact with eyes or mucous membranes, damaged skin or wounds. do not use if you are allergic to Arnica montana or to any of this product's inactive ingredients. If pregnant or breast feeding, ask a physician before use. Keep out of reach of children and pets, if swallowed, seek professional help and contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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