ICE MUSCLE RUB Leon M.C

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: ICE MUSCLE RUB Leon M.C
Generic name: MENTHOL
Manufacturer: Southern Sales & Service, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4efaf347-7406-4690-8005-e7cf2e3d4222
SPL ID: 0b57d91e-06ca-37f8-e063-6294a90a6515
Version: 8
Effective date: 2023-11-29
Source export date: 2026-10-27
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:43:55

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		ICE MUSCLE RUB Leon M.C	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Southern Sales & Service, Inc.	openfda.manufacturer_name
ndc	package	69822-103-08	openfda.package_ndc
ndc	product	69822-103	openfda.product_ndc
ndc11	package	69822010308	derived:openfda.package_ndc
rxcui		311502	openfda.rxcui
spl id		0b57d91e-06ca-37f8-e063-6294a90a6515	id
spl set id		4efaf347-7406-4690-8005-e7cf2e3d4222	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. When using this product do not bandage tightly do not apply to wounds or damaged skin Stop Use and Ask a Doctor if condition worsens if symptoms persist for more than 7 days or clear up and occur again within a few days"

Reported adverse events (FAERS/openFDA)#

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