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		2026-10-21

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 96 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Pain Relief	MENTHOL 10.5%	CVS	d0ea80ce-38b2-acde-e053-2995a90a47e5	2025-03-31	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	A2A Integrated Pharmaceuticals, LLC	31431866-6fb5-2acd-e063-6294a90ac520	2025-03-31	Warnings	Exact identifier application number: M017
Citrus Cleansing Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	f136616d-9f32-4e55-a495-b7466fd68526	2025-03-28	Warnings	Exact identifier application number: M017
Zpol ULTRA	MENTHOL, METHYL SALICYLATE	Laboratorios Zepol S.A.	1a1433a6-8d04-96df-e063-6394a90a987b	2025-03-27	Warnings	Exact identifier application number: M017
Muscle Recovery Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	1c347267-b653-41bf-9967-7feff17c38af	2025-03-27	Warnings	Exact identifier application number: M017
Soothing Lavender Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	ef26523a-b2f2-466e-89ad-f293cd64decb	2025-03-27	Warnings	Exact identifier application number: M017
Achelon Lidocaine Patch	LIDOCAINE PATCH 4%	Achelon, Inc	31408e21-e58d-6db5-e063-6294a90aa4bc	2025-03-26	Warnings	Exact identifier application number: M017
Achelon Lidocaine Patch	LIDOCAINE PATCH 4%	Achelon, Inc	3143bb72-2969-d66e-e063-6294a90a4604	2025-03-26	Warnings	Exact identifier application number: M017
Parche Leon	CAPSAICIN, CAMPHOR, MENTHOL	Pharmadel LLC	a8f266fa-6e43-559e-e053-2995a90a2c75	2025-03-26	Warnings	Exact identifier application number: M017
Adellina Numbing Cream	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	314a83fe-8bdb-766f-e063-6294a90a61c6	2025-03-26	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Plus Menthol Patch	LIDOCAINE AND MENTHOL	Veridian Healthcare	312f15fe-9297-2dc2-e063-6294a90a6f4d	2025-03-25	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Patch	LIDOCAINE 4%	Veridian Healthcare	3130729d-1679-90cd-e063-6294a90a21e6	2025-03-25	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Patch	LIDOCAINE 4%	Veridian Healthcare	31314dda-6199-574d-e063-6394a90aae7a	2025-03-25	Warnings	Exact identifier application number: M017
RWSEFK Lidocaine Pain Relief Gel-Patch	LIDOCAINE PAIN RELIEF GEL-PATCH	Henan Enokon Medical Instrument Co., Ltd.	31366793-f8a6-a2c4-e063-6294a90acbfc	2025-03-25	Warnings	Exact identifier application number: M017
Forticept Wounds and Burns Hydrogel	BENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	Lidan, inc.	c6f58b63-9838-4ff4-8b1a-de2d41d6cf5f	2025-03-25	Warnings	Exact identifier application number: M017
MQ Pain Relieving Patch	PAIN RELIEVING PATCH	Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	0978ff22-c357-e266-e063-6394a90a98a4	2025-03-24	Warnings	Exact identifier application number: M017
LidoPro Patch (Lidocaine 4%, Menthol 1%)	LIDOCAINE AND MENTHOL PATCH	Advanced Rx of Tennessee, LLC	30c97646-db06-df84-e063-6394a90a7743	2025-03-20	Warnings	Exact identifier application number: M017
Carmex Classic Lip Balm Medicated	CAMPHOR (SYNTHETIC), PETROLATUM	Carma Laboratories, Inc.	fb6eb93b-7dc0-4b6f-bfe1-1a7b47588e57	2025-03-20	Warnings	Exact identifier application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Daily Care Lip Balm SPF	CAMPHOR (SYNTHETIC), WHITE PETROLATUM OCTINOXATE, OXYBENZONE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Carma Laboratories, Inc.	5f904369-5f21-4907-98de-df23bce30823	2025-03-20	Warnings	Exact identifier application number: M017
DermaCort Anti-itch	HYDROCORTISONE	Melaleuca, Inc.	24044b0f-dd1e-4762-82b8-7a28b08c2f77	2025-03-20	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