Mountain Ice

Product NDC: 72793-100
11-digit product format: 727930100
Labeler code: 72793
Product ID: 72793-100_3d702bcc-f0aa-e849-e063-6294a90a7fc6
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Mountainside Medical Equipment, Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-05-28
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 5 g/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72793-100	72793-100-02	D	Discontinued by firm		2026-10-23

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Mountain Ice
Brand name suffix: Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	5 g/100mL

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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
415975	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
c79fdd91-16f4-4ae0-bee4-d37c05ed2074	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72793-100-01	Mountain IcePain Relief	118 mL in 1 TUBE	GEL	118	6
72793-100-02	Mountain IcePain Relief	30 mL in 1 BOTTLE, PUMP	GEL	30	6
72793-100-03	Mountain IcePain Relief	946 mL in 1 BOTTLE, PUMP	GEL	946	6
72793-100-04	Mountain IcePain Relief	6 mL in 1 PACKET	GEL	6	6
72793-100-05	Mountain IcePain Relief	99 mL in 1 BOTTLE, WITH APPLICATOR	GEL	99	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72793-100	MOUNTAIN ICE PAIN RELIEF (MENTHOL) GEL [MOUNTAINSIDE MEDICAL EQUIPMENT, INC.]	4	Current NDC, Legacy NDC, 5 package rows	20231228_c79fdd91-16f4-4ae0-bee4-d37c05ed2074.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 117 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MYCO Clinic Pain Relief	MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	604a30c9-2306-47a1-bd31-94b63639dd90	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	0b489420-3b5c-43c5-aab4-0e3720acf9ce	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	dd906129-a787-4352-856d-d7a915031a6e	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Arthritis Pain Relief Cream	HISTAMINE DIHYDROCHLORIDE	Walgreens Company	80d3031a-7fa9-4f5b-b85e-c7c6ef314801	2024-11-20	Warnings	Exact identifier application number: M017
Anti-Itch Medicated Maximum Strength	BENZOCAINE AND RESORCINOL	Walgreens Company	7fd86dcb-edef-4d0d-b389-7ecea595fe67	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Pain Relief	BENZOCAINE	Walgreens Company	7cee7234-32cd-4bf3-8a6c-0882585eec7f	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Advanced Scar Gel	ADVANCED SCAR GEL	Walgreens Company	2c040475-a124-485c-933e-66b452f5ab46	2024-11-20	Warnings	Exact identifier application number: M017
LidoPro Pain Relief	CAPSAICIN AND LIDOCAINE	Clinic Pharma	274611ea-7fc2-ba3f-e063-6294a90aa50f	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief Pad	BENZOCAINE	Acme United Corporation	5087cbbd-1bbe-62ed-e054-00144ff8d46c	2024-11-19	Warnings	Exact identifier application number: M017
Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Acme United Corporation	6bb9a782-2394-4c8c-e053-2991aa0a08d4	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief	BENZOCAINE	Acme United Corporation	697127d1-c02e-16d2-e053-2a91aa0a39fd	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Hydrocortisone 1% Anti-Itch	HYDROCORTISONE	Acme United Corporation	e5597b11-b08e-99e1-e053-2a95a90a15a5	2024-11-19	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Roll-on Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	4115f0ac-e12a-4e59-94f5-a47dcc7f8766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	ac6c2112-8692-4628-97d8-3a5a9f509766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Odor-Free Therapy Arthritis Analgesic	TROLAMINE SALICYLATE	Wal-Mart Stores, Inc.	1d73e7b6-c7f9-4680-b3e3-a954b91e1863	2024-11-18	Warnings	Exact identifier application number: M017
First Aid Only Burn	LIDOCAINE HYDROCHLORIDE	Acme United Corporation	9af39fcd-0a57-26d0-e053-2a95a90a99a0	2024-11-17	Warnings	Exact identifier application number: M017
First Aid Only First Aid/Burn	LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	Acme United Corporation	caa67a05-bdbd-c380-e053-2995a90a0bf1	2024-11-17	Warnings	Exact identifier application number: M017
Meijer Pain Lidocaine Plus Relieving Analgesic	BENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDE	Meijer Distribution, Inc	b7385140-3f63-4cbc-b557-de1d29d1ea36	2024-11-15	Warnings	Exact identifier application number: M017
Signature Care Hydrocortisone	HYDROCORTISONE	Safeway	c6b9c4e1-bab8-490d-8c00-c43377ad0857	2024-11-15	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Walgreen Company	1a9b8b4c-3e15-49e6-af91-76ed0dc0829e	2024-11-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
415975	menthol 5 % Topical Gel	PSN	c79fdd91-16f4-4ae0-bee4-d37c05ed2074	6
415975	menthol 0.05 MG/MG Topical Gel	SCD	c79fdd91-16f4-4ae0-bee4-d37c05ed2074	6
415975	menthol 5 % Topical Gel	SY	c79fdd91-16f4-4ae0-bee4-d37c05ed2074	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72793-100-01	72793010001	118 mL in 1 TUBE (72793-100-01)	118 ml	2019-05-28	0000-00-00	No	No	Current
72793-100-02	72793010002	30 mL in 1 BOTTLE, PUMP (72793-100-02)	30 ml	2019-05-28	0000-00-00	No	No	Current
72793-100-03	72793010003	946 mL in 1 BOTTLE, PUMP (72793-100-03)	946 ml	2019-12-06	0000-00-00	No	No	Current
72793-100-04	72793010004	6 mL in 1 PACKET (72793-100-04)	6 ml	2019-12-06	0000-00-00	Yes	No	Current
72793-100-05	72793010005	99 mL in 1 BOTTLE, WITH APPLICATOR (72793-100-05)	99 ml	2020-05-04	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Mountain Ice Pain Relief Gel	Mountainside Medical Equipment, Inc. \| Fragrance Manufacturing, Inc.	2025-08-28	HUMAN OTC DRUG LABEL	6