THE GOO MEDICATED 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: THE GOO MEDICATED PAIN RELIEF
Generic name: METHYL SALICYLATE, MENTHOL, CAMPHOR
Manufacturer: APSM PERFORMANCE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: db4c321c-8cdc-5a11-e053-2995a90a91a1
SPL ID: 4914f51b-96e4-989e-e063-6394a90a424f
Version: 3
Effective date: 2026-01-23
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:34

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		THE GOO MEDICATED PAIN RELIEF	openfda.brand_name
generic name		METHYL SALICYLATE, MENTHOL, CAMPHOR	openfda.generic_name
manufacturer name		APSM PERFORMANCE, LLC	openfda.manufacturer_name
ndc	package	82503-101-11	openfda.package_ndc
ndc	product	82503-101	openfda.product_ndc
ndc11	package	82503010111	derived:openfda.package_ndc
rxcui		1116730	openfda.rxcui
spl id		4914f51b-96e4-989e-e063-6394a90a424f	id
spl set id		db4c321c-8cdc-5a11-e053-2995a90a91a1	set_id
unii		75IZZ8Y727	openfda.unii
unii		L7T10EIP3A	openfda.unii
unii		LAV5U5022Y	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 Avoid contact with eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not use in large quantities, particularly over raw surfaces or blistered areas.

Reported adverse events (FAERS/openFDA)#

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