blue goo Pain Relieving

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: blue goo Pain Relieving
Generic name: MENTHOL 2.5%
Manufacturer: Garcoa, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7b9b5ac6-9568-464c-8096-0302a1e650df
SPL ID: 0442588a-78e5-4733-8392-1b380f4d8a17
Version: 1
Effective date: 2026-02-13
Source export date: 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:32:02

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		blue goo Pain Relieving	openfda.brand_name
generic name		MENTHOL 2.5%	openfda.generic_name
manufacturer name		Garcoa, Inc.	openfda.manufacturer_name
ndc	package	67385-883-02	openfda.package_ndc
ndc	package	67385-883-01	openfda.package_ndc
ndc	package	67385-883-03	openfda.package_ndc
ndc	product	67385-883	openfda.product_ndc
ndc11	package	67385088301	derived:openfda.package_ndc
ndc11	package	67385088303	derived:openfda.package_ndc
ndc11	package	67385088302	derived:openfda.package_ndc
spl id		0442588a-78e5-4733-8392-1b380f4d8a17	id
spl set id		7b9b5ac6-9568-464c-8096-0302a1e650df	set_id
unii		L7T10EIP3A	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 •Do not apply to wounds or damaged skin • Do not bandage tightly •Do not use with heating pads or heating devices •Discontinue use and consult a doctor if condition worsens or if symptoms persist for 7 days or more or clear up and occur again within a few days, or if pain, swelling or redness occurs after continued use

Reported adverse events (FAERS/openFDA)#

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