Fast Freeze

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: Fast Freeze
Generic name: MENTHOL
Manufacturer: Natural Essentials Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a96e3e41-871c-4cf3-93b6-af2a6246ded8
SPL ID: 23a8b4cf-a5ed-57c9-e063-6394a90a494b
Version: 4
Effective date: 2024-10-04
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:25:38

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Fast Freeze	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Natural Essentials Inc.	openfda.manufacturer_name
ndc	package	66902-016-05	openfda.package_ndc
ndc	package	66902-016-04	openfda.package_ndc
ndc	package	66902-016-16	openfda.package_ndc
ndc	package	66902-016-32	openfda.package_ndc
ndc	package	66902-016-03	openfda.package_ndc
ndc	package	66902-016-01	openfda.package_ndc
ndc	product	66902-016	openfda.product_ndc
ndc11	package	66902001632	derived:openfda.package_ndc
ndc11	package	66902001603	derived:openfda.package_ndc
ndc11	package	66902001601	derived:openfda.package_ndc
ndc11	package	66902001616	derived:openfda.package_ndc
ndc11	package	66902001604	derived:openfda.package_ndc
ndc11	package	66902001605	derived:openfda.package_ndc
rxcui		808955	openfda.rxcui
rxcui		1365998	openfda.rxcui
spl id		23a8b4cf-a5ed-57c9-e063-6394a90a494b	id
spl set id		a96e3e41-871c-4cf3-93b6-af2a6246ded8	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 Do not use With heating pad or device With ointments, creams, sprays or liniments On wounds, damaged skin or irritated skin Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding When using this product Avoid contact with eyes or mucous membranes Do not bandage tightly Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up then reoccur again within a few days Irritation develops Keep out of 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.