FDA.reportPublic FDA data

NDC 52000-072-01 - Muscle Rub Pain Reliever Gel

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
52000-072
Requested NDC
52000-072-01
Package NDCs from labels
52000-072-03, 52000-072-04, 52000-072-01, 52000-072-02
Manufacturer
Universal Distribution Centre LLC
Effective date
2025-10-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLCUniversal Distribution Centre LLC2025-10-30HUMAN OTC DRUG LABEL
Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLCUniversal Distribution Centre LLC2024-12-03HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52000-072-022025-07-29C16284748780-13b156c62-308b-fb37-e063-e6dba90a4e07Pain Reliever Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-072-01Muscle Rub Pain Reliever Gel35.4 g in 1 TUBEGEL35.44
52000-072-02Muscle Rub Pain Reliever Gel1 in 1 CARTONGEL14
52000-072-03Muscle Rub Pain Reliever Gel35.4 g in 1 TUBEGEL35.43
52000-072-04Muscle Rub Pain Reliever Gel1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-072MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC]4Current NDC, Legacy NDC, 2 package rows20241212_b9a563b6-7988-79df-e053-2995a90a752b.zip
52000-072MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC]2Current NDC, Legacy NDC, 2 package rows20241218_18536e21-afc3-8447-e063-6394a90aabae.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 52 of 239 · 4,773 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mouth RinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLUnited Natural Foods, Inc. dba UNFId9c48c72-b9df-4b3a-bc56-d887196521e22026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLUnited Natural Foods, Inc. dba UNFIcd2b55e5-f69c-425e-84db-d114ba8566722026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Tartar control plusEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLUnited Natural Foods, Inc. dba UNFI263bed7e-b0fa-4a89-a4bd-4e6ae1e106872026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLStrategic Sourcing Services LLCbd54bf7a-2304-4c3f-9cd2-bafea217466e2026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Eucalyptol, Menthol, Methyl salicylate, ThymolEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLStrategic Sourcing Services LLC1de7b114-37a4-4739-a241-7fc8e57066b42026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Eucalyptol, Menthol, Methyl Salicylate, ThymolEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLStrategic Sourcing Services LLC454065e4-5ccf-4c01-861b-8f0ca2cd23b62026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Eucalyptol, Menthol, Methyl Salicylate, ThymolEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLStrategic Sourcing Services LLC03c7e7f3-f72d-49c8-96ca-1d7422413ab42026-02-17Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
HydrocortisoneHYDROCORTISONEMedrock Pharmacy LLC43e00e17-1a48-43db-9589-834568917bbf2026-02-17WarningsExact identifier
application number: M017
Tylenol Precise Cooling Pain RelievingLIDOCAINE, MENTHOLKenvue Brands LLCfc0a3404-b174-3952-e053-6294a90a1e022026-02-16WarningsExact identifier
application number: M017
unii: L7T10EIP3A
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLValu Merchandisers Company117b44ba-5313-40f6-97c4-035a7f039fae2026-02-16Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Aloe Vera GelLIDOCAINE HCLValu Merchandisers Company87ee2b4f-d640-4cec-9f48-1d8aa54434e92026-02-16Warnings, Adverse reactionsExact identifier
application number: M017
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLValu Merchandisers Companyb6144732-99da-4be2-88e0-75f31b323d382026-02-16Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
AntisepticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLValu Merchandisers Company93992f56-2e13-40d8-8e27-1f3989dd4c632026-02-16Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLValu Merchandisers Companyd0ff1845-b937-457d-a6f0-b0c875f12c812026-02-16Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
Isopropyl AlcoholISOPROPYL ALCOHOLValu Merchandisers Companya631c976-cb9b-4099-8630-2a10c14bd3bd2026-02-16Warnings, Adverse reactionsExact identifier
unii: ND2M416302
70%ISOPROPYL ALCOHOLValu Merchandisers Companybe57aa83-f097-4ff8-81f8-13d731eea4e62026-02-16Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLValu Merchandisers Company81b5a92a-27a9-41d2-bc88-920833be66382026-02-16Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Hemp Magic Fast-Acting Pain Relief CreamMENTHOLNexxus Capital LLC4af69640-1413-868b-e063-6394a90a39892026-02-16WarningsExact identifier
application number: M017
unii: L7T10EIP3A
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLUnited Natural Foods, Inc. dba UNFIcce74940-ebf1-4fa4-9ef4-50619704d5cd2026-02-16Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
RelaxInk LIDOCAINELIDOCAINE 4%Hambli Limited49a1cf66-9bb1-b918-e063-6394a90a2ff62026-02-15WarningsExact identifier
application number: M017

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.