Ice Quake

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 Quake
Generic name: MENTHOL
Manufacturer: Southern Sales & Service, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7a05832f-49ac-4013-b240-4405501e45cd
SPL ID: 0b57cdd0-d6ef-4e06-e063-6294a90a5af5
Version: 8
Effective date: 2023-11-29
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 05:44:12

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 Quake	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Southern Sales & Service, Inc.	openfda.manufacturer_name
ndc	package	69822-100-04	openfda.package_ndc
ndc	product	69822-100	openfda.product_ndc
ndc11	package	69822010004	derived:openfda.package_ndc
rxcui		1311523	openfda.rxcui
spl id		0b57cdd0-d6ef-4e06-e063-6294a90a5af5	id
spl set id		7a05832f-49ac-4013-b240-4405501e45cd	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 Avoid contact with eyes. For external use only. 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 symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. If 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.