FDA.reportPublic FDA data

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
IngredientStrength
MENTHOL, UNSPECIFIED FORM80 mg/g
METHYL SALICYLATE300 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup
LAV5U5022YInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
311511Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f5684158-0d83-4031-b493-5422ddc73e78Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-2002-42023-02-07C16284748780-1f386c649-9e7e-0266-e053-dadaa90a7c1aDrug Facts - Mentholatum Deep Heating Rub
10742-2002-42023-01-30C16284748780-1f386c649-9e7e-0266-e053-dadaa90a7c1aDrug Facts - Mentholatum Deep Heating Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-2002-4Mentholatum Deep Heating RubExtra Strength57 g in 1 TUBECREAM579
10742-2002-4Mentholatum Deep Heating RubExtra Strength2 in 1 CARTONCREAM29

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3AMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022YMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
MENTHOLACTIVE MOIETYL7T10EIP3AMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE4MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
POLOXAMER 407INACTIVE INGREDIENTTUF2IVW3M2MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
QUATERNIUM-15INACTIVE INGREDIENTE40U03LEM0MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
SORBITAN MONOSTEARATEINACTIVE INGREDIENTNVZ4I0H58XMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2
WATERINACTIVE INGREDIENT059QF0KO0RMENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-2002MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY]9Current NDC, Legacy NDC, 2 package rows20241215_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 97 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Muscle Recovery Foot Soak and Body SoakCAMPHORSANSAR, LLC1c347267-b653-41bf-9967-7feff17c38af2025-03-27WarningsExact identifier
application number: M017
Soothing Lavender Foot Soak and Body SoakCAMPHORSANSAR, LLCef26523a-b2f2-466e-89ad-f293cd64decb2025-03-27WarningsExact identifier
application number: M017
Achelon Lidocaine PatchLIDOCAINE PATCH 4%Achelon, Inc31408e21-e58d-6db5-e063-6294a90aa4bc2025-03-26WarningsExact identifier
application number: M017
Achelon Lidocaine PatchLIDOCAINE PATCH 4%Achelon, Inc3143bb72-2969-d66e-e063-6294a90a46042025-03-26WarningsExact identifier
application number: M017
Parche LeonCAPSAICIN, CAMPHOR, MENTHOLPharmadel LLCa8f266fa-6e43-559e-e053-2995a90a2c752025-03-26WarningsExact identifier
application number: M017
Adellina Numbing CreamLIDOCAINEGuangzhou Haishi Biological Technology Co., Ltd.314a83fe-8bdb-766f-e063-6294a90a61c62025-03-26WarningsExact identifier
application number: M017
HealthWise Lidocaine Plus Menthol PatchLIDOCAINE AND MENTHOLVeridian Healthcare312f15fe-9297-2dc2-e063-6294a90a6f4d2025-03-25WarningsExact identifier
application number: M017
HealthWise Lidocaine PatchLIDOCAINE 4%Veridian Healthcare3130729d-1679-90cd-e063-6294a90a21e62025-03-25WarningsExact identifier
application number: M017
HealthWise Lidocaine PatchLIDOCAINE 4%Veridian Healthcare31314dda-6199-574d-e063-6394a90aae7a2025-03-25WarningsExact identifier
application number: M017
RWSEFK Lidocaine Pain Relief Gel-PatchLIDOCAINE PAIN RELIEF GEL-PATCHHenan Enokon Medical Instrument Co., Ltd.31366793-f8a6-a2c4-e063-6294a90acbfc2025-03-25WarningsExact identifier
application number: M017
Forticept Wounds and Burns HydrogelBENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDELidan, inc.c6f58b63-9838-4ff4-8b1a-de2d41d6cf5f2025-03-25WarningsExact identifier
application number: M017
MQ Pain Relieving PatchPAIN RELIEVING PATCHZhengzhou Miaoqi Pharmaceutical Technology Co., Ltd0978ff22-c357-e266-e063-6394a90a98a42025-03-24WarningsExact identifier
application number: M017
LidoPro Patch (Lidocaine 4%, Menthol 1%)LIDOCAINE AND MENTHOL PATCHAdvanced Rx of Tennessee, LLC30c97646-db06-df84-e063-6394a90a77432025-03-20WarningsExact identifier
application number: M017
Carmex Classic Lip Balm MedicatedCAMPHOR (SYNTHETIC), PETROLATUMCarma Laboratories, Inc.fb6eb93b-7dc0-4b6f-bfe1-1a7b47588e572025-03-20WarningsExact identifier
application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Daily Care Lip Balm SPFCAMPHOR (SYNTHETIC), WHITE PETROLATUM OCTINOXATE, OXYBENZONE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENECarma Laboratories, Inc.5f904369-5f21-4907-98de-df23bce308232025-03-20WarningsExact identifier
application number: M017
DermaCort Anti-itchHYDROCORTISONEMelaleuca, Inc.24044b0f-dd1e-4762-82b8-7a28b08c2f772025-03-20WarningsExact identifier
application number: M017
AUVON Lidocaine Menthol Pain Relief PatchLIDOCAINE AND MENTHOLSHENZHEN YUWEN E-COMMERCE CO., LTD.300cf469-5ca2-a40d-e063-6294a90a68012025-03-20WarningsExact identifier
application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONECarma Laboratories, Inc.3a3af6e1-0281-462e-85e7-144cc5d46f322025-03-19WarningsExact identifier
application number: M017
Lidocaine 4%LIDOCAINEInnovida Pharmaeutique Corporationeb83a3dd-557e-4334-b806-5fc05e9175a32025-03-19WarningsExact identifier
application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONECarma Laboratories, Inc.c04059e9-8175-46c2-8582-f84ef193abd32025-03-19WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311511menthol 8 % / methyl salicylate 30 % Topical CreamPSNf5684158-0d83-4031-b493-5422ddc73e789
311511menthol 80 MG/ML / methyl salicylate 300 MG/ML Topical CreamSCDf5684158-0d83-4031-b493-5422ddc73e789
311511menthol 8 % / methyl salicylate 30 % Topical CreamSYf5684158-0d83-4031-b493-5422ddc73e789

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-2002-4107422002042 TUBE in 1 CARTON (10742-2002-4) / 57 g in 1 TUBE2 tube1992-12-150000-00-00NoNoCurrent