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		2026-10-15

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 15 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lidocaine and Menthol	LIDOCAINE AND MENTHOL	Advanced Rx of Tennessee, LLC	44840250-2112-6ef4-e063-6394a90acdcc	2026-06-12	Warnings	Exact identifier application number: M017
DRAWYUM Pain Relief Gel-Patch	LIDOCAINE 4% PAIN RELIEF GEL-PATCH	Jiangxi Yudexi Pharmaceutical Co., LTD	497e6e18-ba46-0001-e063-6294a90af026	2026-06-12	Warnings	Exact identifier application number: M017
NATUHEAL JOINT BACK PAIN RELIEF	ARNICA MONTANA HPUS 7% JOINT BACK PAIN RELIEF	Jiangxi Yudexi Pharmaceutical Co., LTD	4c923afa-4d1e-0776-e063-6294a90a2f54	2026-06-12	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	Aldermed Inc.	4a7b532e-b292-b595-e063-6394a90acc9c	2026-06-12	Warnings	Exact identifier application number: M017
MG PLUS MENTHOL	MENTHOL	RENU LABORATORIES, LLC	53737365-b985-3800-e063-6294a90a37f2	2026-06-11	Warnings	Exact identifier application number: M017
CeraVe Developed with Dermatologists Itch Relief Moisturizing	PRAMOXINE HYDROCHLORIDE	L'Oreal USA Products Inc	7c78d980-fc94-498c-aec5-464c0c76c8f4	2026-06-11	Warnings	Exact identifier application number: M017
ANIXIKE Numbing	LIDOCAINE4% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a47f1ed-d8cf-3b0b-e063-6394a90a932a	2026-06-11	Warnings	Exact identifier application number: M017
Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride	PRAMOXINE HYDROCHLORIDE	The Honey Pot Company LLC	81ab7fa7-d9b0-49dc-9782-02f37e588c5e	2026-06-10	Warnings	Exact identifier application number: M017
HealthWise Pain Relief Cream with Lidocaine	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	ef176d33-10b9-ddb2-e053-2995a90a76e3	2026-06-10	Warnings	Exact identifier application number: M017
Warm Patch Tong Gu Huo Luo Gao	PAIN PATCH	Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory	6906c4a0-1557-45e3-b915-80e4dd652ee7	2026-06-10	Warnings	Exact identifier application number: M017
LidoMedix	LIDOCAINE, MENTHOL, CAMPHOR	Absolute Therapeutics, LLC	53d504ef-eea3-6a47-e063-6394a90a1f65	2026-06-09	Warnings	Exact identifier application number: M017
good sense anti itch	HYDROCORTISONE	Preferred Pharmaceuticals Inc.	e51047da-8e17-4dd7-be3c-54820a7485f2	2026-06-09	Warnings	Exact identifier application number: M017
Terramed Just Think Comfort GynoCare BV Guard Intimate Wash	PRAMOXINE HYDROCHLORIDE	Rida LLC	09964550-049c-4c3b-817d-37e660c2e45c	2026-06-08	Warnings	Exact identifier application number: M017
Quality Choice Lidocaine Pain Relief Patch	LIDOCAINE	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	526abe69-4bbc-6e73-e063-6394a90ad25d	2026-06-08	Warnings	Exact identifier application number: M017
Dcsily Numbing Cream	LIDOCAINE	Shenzhen Xinxin Yunhai Technology Co., Ltd.	53cab09c-6d5d-471e-e063-6294a90aa977	2026-06-08	Warnings	Exact identifier application number: M017
Easment 0.1% Capsaicin cream for sensitive skin	CAPSAICIN 0.1%	Easment LLC	537e0106-9e1c-66b8-e063-6294a90ac538	2026-06-05	Warnings	Exact identifier application number: M017
Maximum Strength Pain Relief	MENTHOL CREAM	OWELL NATURALS LLC	5388f2c5-8cfd-a601-e063-6294a90a2e5f	2026-06-04	Warnings	Exact identifier application number: M017
MG PLUS ROLL ON	MENTHOL ROLL ON	RENU LABORATORIES, LLC	535dc42f-38c7-2afc-e063-6294a90ae23d	2026-06-03	Warnings	Exact identifier application number: M017
OP First Aid Series Insect Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Yiwu Ori-Power Medtech Co.,Ltd.	b43af183-834a-0f64-e053-2995a90a3218	2026-06-03	Warnings	Exact identifier application number: M017
PURE PRIMAL DELAY	LIDOCAINE HCL	Prodigy Media Inc	1ddab664-7c44-452f-854f-e386cd69505e	2026-06-03	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