Murasaki Beauty Arnica Bruise Cream

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
Murasaki Beauty Arnica Bruise Cream
Generic name
ARNICA MONTANA 1.5%
Manufacturer
Excelsior Commercial Inc
Product type
HUMAN OTC DRUG
SPL set ID
4340b0d2-e350-59bf-e063-6394a90aaccb
SPL ID
55679209-6e2c-384f-e063-6394a90ac1f1
Version
3
Effective date
2026-06-29
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:47:45
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

For external use only if you are allergic to Arnica Montana or any inactive ingredients in this product. Condition persists for more than 3 days or worsens Symptoms clear up and occur again within a few days avoid contact with eyes, mucous membraneswounds, damaged or irritated skin. Use only as directed. Do not tightly wrap or bandage the treated area. Do not apply heat or ice to the treated area immediately before or after use. lf swallowed, seek medical advice immediately or contact a Poison Control Center right away.(1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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