Fast Freeze

Product NDC: 66902-015
11-digit product format: 669020015
Labeler code: 66902
Product ID: 66902-015_3c31cff6-6674-9ee4-e063-6294a90a6165
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: SPRAY
Route: TOPICAL
Labeler: Natural Essentials Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-01-01
Substance: MENTHOL
Active strength: 100 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	66902-015	66902-015-16	D	Discontinued by firm		2026-10-20
excluded package	package	66902-015	66902-015-27	D	Discontinued by firm		2026-10-20

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	66902-015-27	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	66902-015-16	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	66902-015-27	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	66902-015-16	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Fast Freeze
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	100 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
667889	Internal RxNorm lookup
1365995	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d8c42c8d-6ce0-43bf-b165-41979f3d8f79	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
66902-015-04	Fast Freeze	118 mL in 1 BOTTLE, PUMP	SPRAY	118	6
66902-015-12	Fast Freeze	118 mL in 1 BOTTLE	SPRAY	118	6
66902-015-12	Fast Freeze	12 in 1 CASE	SPRAY	12	6
66902-015-16	Fast Freeze	1 mL in 1 BOTTLE, PUMP	SPRAY	1	6
66902-015-27	Fast Freeze	1 mL in 1 BOTTLE, PUMP	SPRAY	1	6
66902-015-44	Fast Freeze	118 mL in 1 CAN	SPRAY	118	6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
.ALPHA.-TOCOPHEROL ACETATE	INACTIVE INGREDIENT	9E8X80D2L0	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
ILEX PARAGUARIENSIS LEAF	INACTIVE INGREDIENT	1Q953B4O4F	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66902-015	FAST FREEZE (MENTHOL) SPRAY [NATURAL ESSENTIALS INC.]	4	Current NDC, Legacy NDC, 6 package rows	20241006_d8c42c8d-6ce0-43bf-b165-41979f3d8f79.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 124 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Wegmans Aloe After Sun Gel with Lidocaine HCl External Analgesic	LIDOCAINE HYDROCHLORIDE	WEGMANS FOOD MARKETS INC	f70bc438-7ed8-f74d-e053-6394a90a2b3f	2024-10-16	Warnings	Exact identifier application number: M017
EQUATE Sunburn relief with Aloe After Sun	LIDOCAINE	Wal-Mart Stores Inc	c25e1288-7ac6-41fc-ab65-26c379f288a7	2024-10-16	Warnings	Exact identifier application number: M017
Genuine First Aid Insect Sting Relief Pad 1 ct	BENZOCAINE, ALCOHOL	GFA Production (Xiamen) Co., Ltd.	b119ba37-0ee1-851a-e053-2995a90a85b1	2024-10-15	Warnings	Exact identifier application number: M017
PAIN RELIEF PATCHES	LIDOCAINE	Walgreen Company	1a587e6e-88d1-4b01-abad-9a365dc64a4d	2024-10-15	Warnings	Exact identifier application number: M017
TopCare Everyday After Sun Cooling	LIDOCAINE HYDROCHLORIDE	TOPCO ASSOCIATES LLC	baff7293-e1a3-d1f2-e053-2995a90a93ca	2024-10-15	Warnings	Exact identifier application number: M017
Universal PAIN RELIEF	LIDOCAINE	Universal Distribution Center LLC	b132a4f2-1b1f-4e80-a183-f9add449065f	2024-10-14	Warnings	Exact identifier application number: M017
Nervex Pain Relieving	CAPSAICIN	VITA SCIENCES, LLC	a39bba22-8c54-4252-9973-052dd2aaea36	2024-10-14	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain-Relieving	LIDOCAINE	NATURAL ESSENTIALS, INC.	d07fdffd-bf7c-4950-9b2d-c06d54ef4c55	2024-10-14	Warnings	Exact identifier application number: M017
Walgreens Cooling	LIDOCAINE HYDROCHLORIDE	WALGREEN COMPANY	baffb272-436c-4ad8-e053-2a95a90a56fb	2024-10-14	Warnings	Exact identifier application number: M017
Walgreens Sunburn Relief	MENTHOL	WALGREEN COMPANY	c8967fba-6c28-494b-e053-2995a90acbba	2024-10-14	Warnings	Exact identifier application number: M017
Walgreens Sunburn Relief	LIDOCAINE	WALGREEN COMPANY	d5067903-c559-dc6d-e053-2995a90a8ee3	2024-10-14	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF	Meijer Distribution Inc	18998e1c-1254-4d0c-93f1-26652c5ca076	2024-10-14	Warnings	Exact identifier application number: M017
signature care itch relief	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Safeway	3eedcd9f-8312-4d14-a0fe-6b00a00d3e73	2024-10-13	Warnings	Exact identifier application number: M017
itch relief	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	H E B	34c7bcd3-203f-4630-894d-3739a1576c8d	2024-10-13	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	H E B	25ec9014-64c4-44df-9e67-9f9223ffc923	2024-10-12	Warnings	Exact identifier application number: M017
PAIN RELIEF Gel-Roll On	LIDOCAINE AND MENTHOL	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	f02fa9c0-b8af-f362-e053-2a95a90ae516	2024-10-11	Warnings	Exact identifier application number: M017
Insect Sting Relief Pad	BENZOCAINE, ALCOHOL	Hubei Changjian Medical Products Co., Ltd.	6a269982-0e25-4c09-aef1-0b398bdc5ed4	2024-10-11	Warnings	Exact identifier application number: M017
HYDROCORTISONE	HYDROCORTISONE	VIVE HEALTH LLC	24221805-e5c9-5785-e063-6394a90a9d2f	2024-10-10	Warnings	Exact identifier application number: M017
De La Cruz Camphor	CAMPHOR	DLC Laboratories, Inc.	62359237-de2d-4497-bfd6-36991cfc8acf	2024-10-10	Warnings	Exact identifier application number: M017
Anti Itch	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Meijer Distribution Inc	4f536a86-6419-4ab0-a7e8-5c37943823e2	2024-10-09	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1365995	FAST FREEZE Naturally Cool 10 % Topical Spray	PSN	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
667889	menthol 10 % Topical Spray	PSN	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
1365995	menthol 100 MG/ML Topical Spray [Fast Freeze Naturally Cool]	SBD	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
667889	menthol 100 MG/ML Topical Spray	SCD	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
1365995	Fast Freeze Naturally Cool 10 % Topical Spray	SY	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
1365995	Fast Freeze Naturally Cool 100 MG/ML Topical Spray	SY	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6
667889	menthol 10 % Topical Spray	SY	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66902-015-04	66902001504	118 mL in 1 BOTTLE, PUMP (66902-015-04)	118 ml	2013-01-01	0000-00-00	No	No	Current
66902-015-12	66902001512	12 BOTTLE in 1 CASE (66902-015-12) / 118 mL in 1 BOTTLE	12 bottle	2025-08-12		No	No	Current
66902-015-16	66902001516	1 g in 1 BOTTLE, PUMP (66902-015-16)	1 g	2013-01-01	0000-00-00	No	No	Current
66902-015-27	66902001527	1 g in 1 BOTTLE, PUMP (66902-015-27)	1 g	2013-01-01	0000-00-00	No	No	Current
66902-015-44	66902001544	118 mL in 1 CAN (66902-015-44)	118 ml	2013-01-01	0000-00-00	No	No	Current