Mentholatum Deep Heating Rub

Product NDC: 10742-2002
11-digit product format: 107422002
Labeler code: 10742
Product ID: 10742-2002_292c797e-751e-ede6-e063-6394a90ae287
Type: HUMAN OTC DRUG
Nonproprietary name: menthol, methyl salicylate
Dosage form: CREAM
Route: TOPICAL
Labeler: The Mentholatum Company
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1992-12-15
Substance: MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength: 80; 300 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Mentholatum Deep Heating Rub
Brand name suffix: Extra Strength
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	80 mg/g
METHYL SALICYLATE	300 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
LAV5U5022Y	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
311511	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
f5684158-0d83-4031-b493-5422ddc73e78	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10742-2002-4	2023-02-07	C162847	48780-1	f386c649-9e7e-0266-e053-dadaa90a7c1a	Drug Facts - Mentholatum Deep Heating Rub
10742-2002-4	2023-01-30	C162847	48780-1	f386c649-9e7e-0266-e053-dadaa90a7c1a	Drug Facts - Mentholatum Deep Heating Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10742-2002-4	Mentholatum Deep Heating RubExtra Strength	57 g in 1 TUBE	CREAM	57		9
10742-2002-4	Mentholatum Deep Heating RubExtra Strength	2 in 1 CARTON	CREAM	2		9

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
GLYCERYL MONOSTEARATE	INACTIVE INGREDIENT	230OU9XXE4	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
QUATERNIUM-15	INACTIVE INGREDIENT	E40U03LEM0	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
SORBITAN MONOSTEARATE	INACTIVE INGREDIENT	NVZ4I0H58X	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10742-2002	MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]	9	Current NDC, Legacy NDC, 2 package rows	20241215_f5684158-0d83-4031-b493-5422ddc73e78.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 128 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Real Time Pain Relief Maxx Topical Analgesic	MENTHOL	REAL TIME PRODUCTS, INC	f45eb95a-2813-4124-bdb0-54e078a8237d	2024-08-20	Warnings	Exact identifier application number: M017
Theracare Lidocaine Pain relief	LIDOCAINE	Veridian Healthcare	1d8a3679-637d-94c0-e063-6294a90a9ecf	2024-08-19	Warnings	Exact identifier application number: M017
LidoSync	LIDOCAINE, MENTHOL	iON Pharma, LLC	200f883c-439a-3b99-e063-6394a90aed10	2024-08-19	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Oil Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	09243a23-1f17-f77b-e063-6394a90a0b22	2024-08-19	Warnings	Exact identifier application number: M017
CVS Health Maximum Strength Scalp Relief Anti-itch	HYDROCORTISONE	CVS Health	b5ef0005-8b76-4205-8be0-db3a7ed7d1c4	2024-08-19	Warnings	Exact identifier application number: M017
Rite Aid Pain Relieving Roll-On	LIDOCAINE HCL	Rite Aid Corporation	1406590c-667c-84eb-e063-6294a90a5052	2024-08-16	Warnings	Exact identifier application number: M017
Nuvira	CAPSAICIN 0.025%, MENTHOL 10%, METHYL NICOTINATE 0.25%, METHYL SALICYLATE 10%	Strand Health Group	ff448183-03cf-df2d-e053-6394a90a77f0	2024-08-16	Warnings	Exact identifier application number: M017
FLANAX	METHYL SALICYLATE, MENTHOL, CAPSAICIN	Belmora LLC	5e06c688-a086-4c1c-8dab-fcead61fef40	2024-08-13	Warnings	Exact identifier application number: M017
Pain Relief	MENTHOL	Pain Relieving Spray Inc.	1f44466f-044f-70fe-e063-6294a90ad575	2024-08-09	Warnings	Exact identifier application number: M017
Meijer Cold Therapy Pain Relieving	MENTHOL	Meijer Inc	1c5b55e3-f859-71b6-e063-6294a90a633b	2024-08-08	Warnings	Exact identifier application number: M017
HealthWise Soothing Cold Therapy Gel	MENTHOL 4%	Veridian Healthcare	1f09ccdd-09d8-6a8d-e063-6394a90a184f	2024-08-08	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Nantong Health & Beyond Hygienic Products Inc.	fbbbcc67-b46d-d41a-e053-6294a90aa55d	2024-08-08	Warnings	Exact identifier application number: M017
Cheezheng Pain Relief Cream	MENTHOL	Tibet Cheezheng Tibetan Medicine Co. Ltd	37279a3f-9207-4e4c-90d6-52735044f104	2024-08-07	Warnings	Exact identifier application number: M017
CVS Health Hydrocortisone Anti Itch	HYDROCORTISONE	CVS Health	546a1b8a-8254-432a-85c4-38ebee5ad568	2024-08-07	Warnings	Exact identifier application number: M017
SANTO REMEDIO Alivio Pain Relieving Lavender Scent	LIDOCAINE HYDROCHLORIDE, MENTHOL	SANTO REMEDIO LLC	ab53c7f2-a768-4f36-89d6-e128a1a940c2	2024-08-05	Warnings	Exact identifier application number: M017
CVS Health Maximum Strength Hydrocortisone	HYDROCORTISONE OINTMENT	CVS Health	ee9ed7ca-1642-4cf6-ae4b-d1c11b37eaf3	2024-08-02	Warnings	Exact identifier application number: M017
Anti-Itch Vulva Cream 1 Hydrocortisone Acetate	HYDROCORTISONE ACETATE	The Honey Pot Company LLC	6f32b536-6ebf-49a8-abb6-2a1daae2f6d7	2024-08-01	Warnings	Exact identifier application number: M017
Anti Itch Soothing 1 Pramoxine Hydrochloride	PRAMOXINE HYDROCHLORIDE	The Honey Pot Company LLC	8bfeea34-25d5-4721-a17f-d9f1d0084cc3	2024-08-01	Warnings	Exact identifier application number: M017
AVON footworks Arthritis Achy Foot and Muscle	METHYL SALICYLATE	The Avon Company	1f440f60-cfc4-511e-e063-6294a90a87db	2024-08-01	Warnings	Exact identifier application number: M017
AVON footworks Maximum Strength Cracked Heel	BENZALKONIUM CHLORIDE, LIDOCAINE	The Avon Company	1f45752e-4a55-431e-e063-6294a90aa57a	2024-08-01	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
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
311511	menthol 8 % / methyl salicylate 30 % Topical Cream	PSN	f5684158-0d83-4031-b493-5422ddc73e78	9
311511	menthol 80 MG/ML / methyl salicylate 300 MG/ML Topical Cream	SCD	f5684158-0d83-4031-b493-5422ddc73e78	9
311511	menthol 8 % / methyl salicylate 30 % Topical Cream	SY	f5684158-0d83-4031-b493-5422ddc73e78	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
10742-2002-4	10742200204	2 TUBE in 1 CARTON (10742-2002-4) / 57 g in 1 TUBE	2 tube	1992-12-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts - Mentholatum Deep Heating Rub	The Mentholatum Company	2024-12-13	HUMAN OTC DRUG LABEL	9