Pain Relief

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: Pain Relief
Generic name: ARNICA, MENTHOL CRYSTALS, CINNAMON, PEPPERMINT, GINGER, ROSEMARY
Manufacturer: Spry Life LLC
Product type: HUMAN OTC DRUG
SPL set ID: 480dc24e-87d0-55db-e054-00144ff88e88
SPL ID: 4604cabb-ce1e-ae65-e063-6394a90a200e
Version: 7
Effective date: 2025-12-15
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:56

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pain Relief	openfda.brand_name
generic name		ARNICA, MENTHOL CRYSTALS, CINNAMON, PEPPERMINT, GINGER, ROSEMARY	openfda.generic_name
manufacturer name		Spry Life LLC	openfda.manufacturer_name
ndc	package	70994-102-01	openfda.package_ndc
ndc	package	70994-102-04	openfda.package_ndc
ndc	package	70994-102-08	openfda.package_ndc
ndc	package	70994-102-10	openfda.package_ndc
ndc	package	70994-102-02	openfda.package_ndc
ndc	package	70994-102-09	openfda.package_ndc
ndc	product	70994-102	openfda.product_ndc
ndc11	package	70994010209	derived:openfda.package_ndc
ndc11	package	70994010210	derived:openfda.package_ndc
ndc11	package	70994010208	derived:openfda.package_ndc
ndc11	package	70994010204	derived:openfda.package_ndc
ndc11	package	70994010201	derived:openfda.package_ndc
ndc11	package	70994010202	derived:openfda.package_ndc
spl id		4604cabb-ce1e-ae65-e063-6394a90a200e	id
spl set id		480dc24e-87d0-55db-e054-00144ff88e88	set_id
unii		OZ0E5Y15PZ	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 Warnings For external use only. ■ Avoid contact with eyes. ■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns ■ Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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