FDA.reportPublic FDA data

Mentholatum Deep Heating Rub

Product NDC
10742-2002
Requested package NDC
10742-2002-4
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 1 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
JenGufun LIDOCAINE KNEE PatchLIDOCAINE KNEE PATCHHenan Kangdi Medical Devices Co., Ltd.5b1d8508-b993-7a8d-e063-6294a90ae3062026-09-10WarningsExact identifier
application number: M017
Wart Corn RemoverSALICYLIC ACIDHONG KONG FOREVER YOUNG TRADING CO., LIMITED5b0cd6e0-f220-4ebd-e063-6294a90ade672026-09-09WarningsExact identifier
application number: M017
Magic CreamPAIN RELIEVING OINTMENTJiangxi Baikang Medical Products Co., Ltd.5b0f2515-47e9-603f-e063-6294a90af9d42026-09-09WarningsExact identifier
application number: M017
Burn GelLIDOCAINE HCITrifecta Pharmaceuticals USA LLCe9d3e9be-1036-fad0-e053-2a95a90a6efe2026-09-09WarningsExact identifier
application number: M017
4% Lidocaine Pain Relief PatchLIDOCAINE 4%Guangxi Keyun E-commerce Co., Ltd.5b197cd8-542f-38b4-e063-6294a90ad7d32026-09-09WarningsExact identifier
application number: M017
Pain Relieving Lidocaine PatchLIDOCAINEYYBA CORPaf8c84fd-224c-72b3-e053-2a95a90a95682026-09-07WarningsExact identifier
application number: M017
American Safety First AidLIDOCAINE HCLOrazen Incea2f776b-dfd0-6ce4-e053-2995a90af0092026-09-07WarningsExact identifier
application number: M017
MEDI-FIRST Topical AnalgesicLIDOCAINE HCIUltra Distributors Incb6f288f7-9ae3-215e-e053-2a95a90aedf62026-09-07WarningsExact identifier
application number: M017
MEDI-FIRSTBENZALKONIUM CHLORIDE, LIDOCAINEOrazen Incf508434f-5948-7134-e053-2a95a90a03d72026-09-05WarningsExact identifier
application number: M017
MEDI-FIRSTBENZALKONIUM CHLORIDE, LIDOCAINEOrazen Incf522fb0b-3d86-b228-e053-2a95a90a55e92026-09-05WarningsExact identifier
application number: M017
SurviveX Anti-itch CreamSURVIVEX HYDROCORTISONENantong Health & Beyond Hygienic Products Inc.5a7a1141-d3b1-0ee8-e063-6294a90a16aa2026-09-04WarningsExact identifier
application number: M017
NeuroNesic Pain Relieving CreamCAPSAICINBlaine Labs Inc.7107c13d-bf59-4c0a-84fe-725a9fca26912026-09-04WarningsExact identifier
application number: M017
Neoteric Diabetic Skin Care 1 oz.DIMETHICONERNA PHARMA LLC5a944486-9591-f583-e063-6394a90aa04b2026-09-03WarningsExact identifier
application number: M017
Equate Menthol Pain RelievingMENTHOLWal-Mart Stores Incd5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc2026-09-03WarningsExact identifier
application number: M017
ZHI TechnologiesLIDOCAINE, MENTHOLZHI Technologies, Inc.6717e995-4d2d-49e8-8ecf-7c62557dfdef2026-09-03WarningsExact identifier
application number: M017
Komxsum LIDOCAINE CreamLIDOCAINE 4% CREAMWenzhou Yuyuan Pharmaceutical Co., Ltd.5a9feae0-9be4-e736-e063-6294a90abe552026-09-03WarningsExact identifier
application number: M017
FREEZE EASE Roll-OnMENTHOLGlobal America Group LLC1869cc0d-a056-45de-aede-23b09b61ed122026-09-02WarningsExact identifier
application number: M017
Gaimoa Lidocaine Pain Relief Gel PatchesLIDOCAINE PAIN RELIEF GEL PATCHESHenan Enokon Medical Instrument Co., Ltd.5a68fe67-5c15-af9a-e063-6294a90a7ec12026-09-01WarningsExact identifier
application number: M017
CVS Cortisone LiquidHYDROCORTISONECVS Pharmacy42df45a9-d449-090a-e063-6394a90a9ee42026-09-01WarningsExact identifier
application number: M017
Ramedica Herbal Wonder BalmCAMPHOR, MENTHOLRamedicare Sdn. Bhd.cfb2ea0e-a1f6-4fdf-b866-346bbe78788f2026-09-01WarningsExact 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