Home NDC 10742-2002 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.
FDA-Initiated Inactive NDC Indexing# 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 Uploaded 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 38 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TheraCare Muscle and Joint Gel Vanishing Scent MENTHOL 2.5% Veridian Healthcare 494d2a85-45a8-12a2-e063-6294a90a391b 2026-01-26 Warnings Exact identifier application number: M017 Lidocaine Pain Relief LIDOCAINE Trifecta Pharmaceuticals USA, LLC. 493c09d0-16d7-7413-e063-6394a90aa052 2026-01-26 Warnings Exact identifier application number: M017 Topcare Medicated Pain Relieving Patch 60ct TOPCARE PAIN RELIEF PATCH EXTRA STRENGTH Topco Associates LLC 4953c12b-ca6d-d21e-e063-6294a90ac990 2026-01-26 Warnings Exact identifier application number: M017 Dr Sabharwals MENTHOL 5% PATCH Dr. Sabharwal's Wound Care 1025b986-a1e5-701d-e063-6294a90a33fd 2026-01-24 Warnings Exact identifier application number: M017 Target Up and Up Pain Relief Menthol Topical Analgesic MENTHOL Target Corporation 4910f32f-c639-0215-e063-6394a90a1c7b 2026-01-23 Warnings Exact identifier application number: M017 Rapidol HYDROCORTISONE Pharmadel LLC 19a1f1e2-bc6b-7153-e063-6294a90ab115 2026-01-23 Warnings Exact identifier application number: M017 CVS 9083 Maximum Strength Lidocaine 4 Pain Relief Patch 1ct Large LIDOCAINE CVS PHARMACY, INC 4914965f-1164-e20e-e063-6294a90ac221 2026-01-23 Warnings Exact identifier application number: M017 THE GOO MEDICATED PAIN RELIEF METHYL SALICYLATE, MENTHOL, CAMPHOR APSM PERFORMANCE, LLC db4c321c-8cdc-5a11-e053-2995a90a91a1 2026-01-23 Warnings Exact identifier application number: M017 Dr Sabharwals LIDOCAINE 4% AND MENTHOL 1% PATCH Dr. Sabharwal's Wound Care 10249d0f-5ee1-6892-e063-6394a90a967e 2026-01-23 Warnings Exact identifier application number: M017 Easment DMSO cream MENTHOL 1.00% Easment LLC 48f5544e-1cfd-864a-e063-6394a90a71f1 2026-01-22 Warnings Exact identifier application number: M017 Aveeno 1% Hydrocortisone Anti-Itch Cream HYDROCORTISONE Kenvue Brands LLC 1ac0ac4e-af76-9a3e-e063-6394a90a1269 2026-01-22 Warnings Exact identifier application number: M017 RAYO ACTIVE ICE MENTHOL, CAMPHOR Quimicas Handal de Centroamerica SA de CV 09e4a36b-020a-c5b1-e063-6394a90a3e31 2026-01-22 Warnings Exact identifier application number: M017 X-Treme Freeze COLD THERAPY GEL Dynarex Corporation 79f0802f-03ad-bf8f-e053-2991aa0ae4b5 2026-01-22 Warnings Exact identifier application number: M017 Anti Itch HYDROCORTISONE HyVee Inc ae31f1f5-db70-45cf-850e-67bfe6860748 2026-01-21 Warnings Exact identifier application number: M017 ULTRA RELIEF MENTHOL, CAMPHOR CHEMCO CORPORATION 48ea80cf-af54-ce5f-e063-6394a90ac493 2026-01-21 Warnings Exact identifier application number: M017 Healthy Back Institute Rub On Relief ANALGESIC Eagle Labs Inc. 17dff3c1-3c0b-16f6-e063-6394a90a3c05 2026-01-21 Warnings Exact identifier application number: M017 Pain Relief ANALGESIC Fullstack Fulfillment 2a433cee-8b6f-c280-e063-6394a90ae25a 2026-01-21 Exact identifier application number: M017 Walgreens Anti Itch Cream ANTI ITCH CREAM Walgreens Company b545553a-283a-48af-adc5-763758a9ff24 2026-01-21 Warnings Exact identifier application number: M017 CVS Health Maximum Strength Lidocaine Pain Relief Cream Plus Menthol LIDOCAINE HCL, MENTHOL CVS Pharmacy 8aaffa3f-f82f-470c-902d-f366f1a66305 2026-01-21 Warnings Exact identifier application number: M017 LIGHTS Instant Sting Relief Pad BENZOCAINE Lights Medical Manufacture Co., Ltd. 28dd82a7-f360-a022-e063-6394a90a3a76 2026-01-21 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# 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