Mountain Ice Sports 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 Sports Pain Relief
Generic name: MENTHOL, CAMPHOR
Manufacturer: Mountainside Medical Equipment, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c1f5512c-67b1-4ff0-b1a5-616e883d436f
SPL ID: 3a73bfc2-eb57-a98f-e063-6394a90af9d1
Version: 4
Effective date: 2025-07-21
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:10

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Mountain Ice Sports Pain Relief	openfda.brand_name
generic name		MENTHOL, CAMPHOR	openfda.generic_name
manufacturer name		Mountainside Medical Equipment, Inc.	openfda.manufacturer_name
ndc	package	72793-200-04	openfda.package_ndc
ndc	package	72793-200-01	openfda.package_ndc
ndc	package	72793-200-02	openfda.package_ndc
ndc	package	72793-200-03	openfda.package_ndc
ndc	product	72793-200	openfda.product_ndc
ndc11	package	72793020002	derived:openfda.package_ndc
ndc11	package	72793020003	derived:openfda.package_ndc
ndc11	package	72793020001	derived:openfda.package_ndc
ndc11	package	72793020004	derived:openfda.package_ndc
rxcui		2393535	openfda.rxcui
spl id		3a73bfc2-eb57-a98f-e063-6394a90af9d1	id
spl set id		c1f5512c-67b1-4ff0-b1a5-616e883d436f	set_id
unii		75IZZ8Y727	openfda.unii
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, or clear up and recur. Keep out the reach of children: If accidentally swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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