Home NDC 53554-020 AMRUTANJAN RELIEF STRONG PAIN BALM
Product NDC 53554-020
11-digit product format 535540020
Labeler code 53554
Product ID 53554-020_73770c61-9c7e-466f-8371-4ad6f652cbb4
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, METHYL SALICYLATE
Dosage form OINTMENT
Route TOPICAL
Labeler AMRUTANJAN HEALTH CARE LIMITED
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-01
Substance MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength .15; .15 g/g; g/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 40 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 AMRUTANJAN RELIEF STRONG PAIN BALM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM .15 g/g METHYL SALICYLATE .15 g/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 1599818 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53554-020-05 AMRUTANJAN RELIEF STRONG PAIN BALM 1 in 1 CARTON OINTMENT 1 16 53554-020-05 AMRUTANJAN RELIEF STRONG PAIN BALM 30 g in 1 JAR OINTMENT 30 16 53554-020-06 AMRUTANJAN RELIEF STRONG PAIN BALM 30 g in 1 BOTTLE, GLASS OINTMENT 30 16 53554-020-06 AMRUTANJAN RELIEF STRONG PAIN BALM 1 in 1 CARTON OINTMENT 1 16 53554-020-10 AMRUTANJAN RELIEF STRONG PAIN BALM 1 in 1 CARTON OINTMENT 1 16 53554-020-10 AMRUTANJAN RELIEF STRONG PAIN BALM 50 g in 1 JAR OINTMENT 50 16 53554-020-11 AMRUTANJAN RELIEF STRONG PAIN BALM 1 in 1 CARTON OINTMENT 1 16 53554-020-11 AMRUTANJAN RELIEF STRONG PAIN BALM 50 g in 1 BOTTLE, GLASS OINTMENT 50 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MENTHOL ACTIVE INGREDIENT L7T10EIP3A AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 METHYL SALICYLATE ACTIVE INGREDIENT LAV5U5022Y AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 MENTHOL ACTIVE MOIETY L7T10EIP3A AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 BUTYLATED HYDROXYTOLUENE INACTIVE INGREDIENT 1P9D0Z171K AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 CETOSTEARYL ALCOHOL INACTIVE INGREDIENT 2DMT128M1S AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 MICROCRYSTALLINE WAX INACTIVE INGREDIENT XOF597Q3KY AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 PARAFFIN INACTIVE INGREDIENT I9O0E3H2ZE AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53554-020 AMRUTANJAN RELIEF STRONG PAIN BALM (MENTHOL, METHYL SALICYLATE) OINTMENT [AMRUTANJAN HEALTH CARE LIMITED] 15 Current NDC, Legacy NDC, 8 package rows 20250501_206d8c1e-eb5b-4ec7-a54e-8defc9fb9d27.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 33 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tylenol Precise Cooling Pain Relieving LIDOCAINE, MENTHOL Kenvue Brands LLC fc0a3404-b174-3952-e053-6294a90a1e02 2026-02-16 Warnings Exact identifier application number: M017 Aloe Vera Gel LIDOCAINE HCL Valu Merchandisers Company 87ee2b4f-d640-4cec-9f48-1d8aa54434e9 2026-02-16 Warnings, Adverse reactions Exact identifier application number: M017 Hemp Magic Fast-Acting Pain Relief Cream MENTHOL Nexxus Capital LLC 4af69640-1413-868b-e063-6394a90a3989 2026-02-16 Warnings Exact identifier application number: M017 RelaxInk LIDOCAINE LIDOCAINE 4% Hambli Limited 49a1cf66-9bb1-b918-e063-6394a90a2ff6 2026-02-15 Warnings Exact identifier application number: M017 blue goo Pain Relieving MENTHOL 2.5% Garcoa, Inc. 7b9b5ac6-9568-464c-8096-0302a1e650df 2026-02-13 Warnings Exact identifier application number: M017 Methyl Salicylate 30 Percent Cream METHYL SALICYLATE Alexso, Inc 1d50ccb2-1a5d-49c7-8524-2f54eed63e85 2026-02-13 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL, MENTHOL, METHYOL SALICYLATE, THYMOL Topco Associates LLC a38e91c1-7ac6-4a7f-a5a2-8d9166b1535a 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Gel Cooling Pain Relief MENTHOL Topco Associates LLC 80962394-a46f-48fd-8e0c-685dd1e500d7 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Banophen DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Major Pharmaceuticals 9758d886-bd58-4eb2-a827-fa8e7fee2b7c 2026-02-13 Warnings Exact identifier application number: M017 Natureplex Hydrocortisone Hydro HYDROCORTISONE Natureplex, LLC 2fc6a148-34bb-4289-8588-32c1bb011b98 2026-02-13 Warnings Exact identifier application number: M017 Capsaicin 0.035 Percent CAPSAICIN Alexso, Inc 6d0bc1cc-e812-4753-b20c-c0357dd6deb5 2026-02-13 Warnings Exact identifier application number: M017 Swiftalyn Numbing Cream LIDOCAINE 4% GENUINE INNOVATION LTD 3f74c4a6-26f0-ddf7-e063-6394a90a1225 2026-02-12 Warnings Exact identifier application number: M017 PHARMBANNER Arnica Bruise Cream ARNICA BRUISE CREAM Shenzhen Xinxin Yunhai Technology Co., Ltd. 3c783061-8e2d-8a84-e063-6394a90a5265 2026-02-12 Warnings Exact identifier application number: M017 ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP MENTHOL, CAMPHOR Worldwide Cosmetics, Inc 459d64a9-0538-57c8-e063-6394a90a6155 2026-02-12 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL Walgreen Co. cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0 2026-02-12 Warnings, Adverse reactions Exact identifier application number: M017 Medicated Body Powder MENTHOL Walmart Stores Inc afd337b7-d76e-f17a-e053-2a95a90abac7 2026-02-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride 2% LIDOCAINE HYDROCHLORIDE Aldermed Inc. 4977b722-d08d-3d9e-e063-6294a90a9035 2026-02-12 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Jell Pharmaceuticals Pvt Ltd 4a8b3f84-8c45-eb94-e063-6394a90a3e73 2026-02-11 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine Patch LIDOCAINE Walgreen Co. 41c4e9fe-e407-b22a-e063-6394a90a4b27 2026-02-10 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE CREAM 1% Aldermed Inc. 4a7f2c0e-5cf3-29cb-e063-6394a90a5d8d 2026-02-10 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 53554-020-03 53554002003 1 JAR in 1 BLISTER PACK (53554-020-03) > 9 g in 1 JAR 1 jar 2020-12-22 0000-00-00 No No Current 53554-020-05 53554002005 1 JAR in 1 CARTON (53554-020-05) / 30 g in 1 JAR 1 jar 2025-05-01 0000-00-00 No No Current 53554-020-06 53554002006 1 BOTTLE, GLASS in 1 CARTON (53554-020-06) / 30 g in 1 BOTTLE, GLASS 2025-05-01 No No Current 53554-020-10 53554002010 1 JAR in 1 CARTON (53554-020-10) / 50 g in 1 JAR 1 jar 2025-05-01 0000-00-00 No No Current 53554-020-11 53554002011 1 BOTTLE, GLASS in 1 CARTON (53554-020-11) / 50 g in 1 BOTTLE, GLASS 2025-05-01 No No Current