Mineral Ice Methol 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: Mineral Ice Methol Pain Relief
Generic name: MENTHOL 10.5 %
Manufacturer: Sunflora Inc
Product type: HUMAN OTC DRUG
SPL set ID: 6ddd9e97-f717-4d5a-9658-26449a3cc831
SPL ID: 55a126b3-450b-885a-e063-6394a90a39ca
Version: 2
Effective date: 2026-07-02
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 05:19:26

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Mineral Ice Methol Pain Relief	openfda.brand_name
generic name		MENTHOL 10.5 %	openfda.generic_name
manufacturer name		Sunflora Inc	openfda.manufacturer_name
ndc	package	73240-905-01	openfda.package_ndc
ndc	product	73240-905	openfda.product_ndc
ndc11	package	73240090501	derived:openfda.package_ndc
rxcui		1489073	openfda.rxcui
spl id		55a126b3-450b-885a-e063-6394a90a39ca	id
spl set id		6ddd9e97-f717-4d5a-9658-26449a3cc831	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

Warning For external use only Flammable When using this product Avoid sprying in eyes, Do not use with heating pads or heating devices. use only as directed, do not bandage tightly or use with heating pad, avoid contact with eyes and mucous membranes, do not apply to wounds or damaged, brocken, or irritating skin, if severe burning sensation occurs, discontinue use immidiately. Stop use and ask doctor if condition worsen, or symptoms persist for more than 7 days or clear up and occur again withing few days

Reported adverse events (FAERS/openFDA)#

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