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 23 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kevo-Prophen JUNIPER TAR Faeve, LLC 4fe773a8-77cd-831e-e063-6294a90ae2ca 2026-04-20 Warnings Exact identifier application number: M017 BeeVenom METHYL SALICYLATE Menper Distributors, Inc. 4fe7a986-336d-ad4e-e063-6294a90a0b8a 2026-04-20 Warnings Exact identifier application number: M017 Benzodent BENZOCAINE Focus Consumer Healthcare, LLC 5fdcb871-d387-6352-e053-2991aa0a09da 2026-04-20 Warnings Exact identifier application number: M017 Tecnu Calagel DIPHENHYDRAMINE HYDROCHLORIDE Tec Laboratories Inc. 8bc9cbfe-1dd4-18ed-e053-2a95a90a7966 2026-04-20 Warnings Exact identifier application number: M017 Aemerry Numbing Cream MENTHOL 5% Da Capo Prima LLC 4fefddaf-19c8-86b4-e063-6294a90abffc 2026-04-20 Warnings Exact identifier application number: M017 Sting Relief Swab BENZOCAINE 4 Visions LLC 4fc7a356-2f1d-85af-e063-6394a90aec6b 2026-04-18 Warnings Exact identifier application number: M017 Equate Lidocaine and Menthol Paraben Free LIDOCAINE 4% PLUS MENTHOL 1% Walmart Stores Inc 4fa917de-bc46-0b8d-e063-6294a90a218a 2026-04-17 Warnings Exact identifier application number: M017 LidoPro LIDOCAINE AND MENTHOL Advanced Rx of Tennessee, LLC 4faa515f-6040-d948-e063-6294a90a187f 2026-04-17 Warnings Exact identifier application number: M017 Coleman Bite and Sting Relief EXTERNAL ANESTHETIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4fadf1f1-478a-5104-e063-6294a90a10cb 2026-04-17 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Universal Distribution Center LLC 4f921ced-7722-cba5-e063-6294a90a650b 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Capsaicin Hot Patch CAPSAICIN Walgreen Co. 41e959d8-f6ac-f5b4-e063-6294a90abd96 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Cold Therapy Pain Relieving Patch MENTHOL Walgreen Co. 41e7574a-348f-8eb8-e063-6294a90a6e90 2026-04-16 Warnings Exact identifier application number: M017 Coleman Sting and Bite Relief EXTERNAL ANALGESIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4f94ab35-3099-716c-e063-6294a90a8bea 2026-04-16 Warnings Exact identifier application number: M017 Kroger Witch Hazel WITCH HAZEL Kroger Co. 461407d0-fbf6-47e9-e063-6394a90a9a83 2026-04-16 Warnings Exact identifier application number: M017 Stopain Extra Strength Gel MENTHOL Troy Manufacturing, Inc. 86fe4e8c-5279-445a-a19a-e694eac785fd 2026-04-16 Warnings Exact identifier application number: M017 Stopain Clinical MENTHOL, UNSPECIFIED FORM Troy Manufacturing, Inc. 4503208f-2808-4727-8066-c431230bd70b 2026-04-16 Warnings Exact identifier application number: M017 EXTRA STRENGTH STOPAIN COLD PAIN RELIEVING ROLL ON MENTHOL TROY MANUFACTURING, INC 895896dc-0762-40a7-8313-cca10ce68984 2026-04-16 Warnings Exact identifier application number: M017 HealthWise Medicated Cold Hot 5% MENTHOL Veridian Healthcare 4f9b1b2d-1acc-e0a7-e063-6394a90aadbc 2026-04-16 Warnings Exact identifier application number: M017 Lidoease 2% LIDOCAINE HCL 2% PureTek Corporation 3ba0c0ff-0f7a-7a29-e063-6294a90a547a 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Lidocaine Pain Relieving Patch Assorted LIDOCAINE Walgreen Co. 41e98f15-669f-4543-e063-6294a90a1ef7 2026-04-15 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