Mountain Ice 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: Mountain Ice Pain Relief
Generic name: MENTHOL
Manufacturer: Mountainside Medical Equipment, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c79fdd91-16f4-4ae0-bee4-d37c05ed2074
SPL ID: 3d702bcc-f0aa-e849-e063-6294a90a7fc6
Version: 6
Effective date: 2025-08-28
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:19

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
application number		M017	openfda.application_number
brand name		Mountain Ice Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Mountainside Medical Equipment, Inc.	openfda.manufacturer_name
ndc	package	72793-100-02	openfda.package_ndc
ndc	package	72793-100-05	openfda.package_ndc
ndc	package	72793-100-04	openfda.package_ndc
ndc	package	72793-100-01	openfda.package_ndc
ndc	package	72793-100-03	openfda.package_ndc
ndc	product	72793-100	openfda.product_ndc
ndc11	package	72793010001	derived:openfda.package_ndc
ndc11	package	72793010004	derived:openfda.package_ndc
ndc11	package	72793010005	derived:openfda.package_ndc
ndc11	package	72793010003	derived:openfda.package_ndc
ndc11	package	72793010002	derived:openfda.package_ndc
rxcui		415975	openfda.rxcui
spl id		3d702bcc-f0aa-e849-e063-6294a90a7fc6	id
spl set id		c79fdd91-16f4-4ae0-bee4-d37c05ed2074	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. Flammable; keep away from excessive heat or open flame. Avoid contact with eyes or mucous membranes. When using this product: Do not apply to wounds, damaged skin, or irritated skin. Do not apply with other creams, ointments, sprays or liniments. Stop use and ask a doctor if: Conditions worsen, skin irritation develops, or condition does not improve after 7 days. Keep out the reach of children: If accidentally swallowed seek medical attention immediately or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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