Arnica gel

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 gel
Generic name: ARNICA
Manufacturer: WALGREENS
Product type: HUMAN OTC DRUG
SPL set ID: b60f9c58-9908-6184-e053-2a95a90aa435
SPL ID: c7171929-a9a4-5078-e053-2995a90a560e
Version: 2
Effective date: 2021-07-15
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:33:39

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Arnica gel	openfda.brand_name
generic name		ARNICA	openfda.generic_name
manufacturer name		WALGREENS	openfda.manufacturer_name
ndc	package	0363-0139-26	openfda.package_ndc
ndc	product	0363-0139	openfda.product_ndc
ndc11	package	00363013926	derived:openfda.package_ndc
spl id		c7171929-a9a4-5078-e053-2995a90a560e	id
spl set id		b60f9c58-9908-6184-e053-2a95a90aa435	set_id
unii		O80TY208ZW	openfda.unii

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 . Avoid contact with eyes, mucous membranes, damaged skin, or wounds. Do not use if you are allergic to Arnica montana or to any of thus product's inactive ingredients. When using this product use only as directed do not bandage tightly or use a heating pad. Stop use and ask a doctor if condition persists for more than 3 days or worsens.

Reported adverse events (FAERS/openFDA)#

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