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
Label	Manufacturer	Effective date	Type
Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLC	Universal Distribution Centre LLC	2025-10-30	HUMAN OTC DRUG LABEL
Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLC	Universal Distribution Centre LLC	2024-12-03	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52000-072-02	2025-07-29	C162847	48780-1	3b156c62-308b-fb37-e063-e6dba90a4e07	Pain Reliever Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52000-072-01	Muscle Rub Pain Reliever Gel	35.4 g in 1 TUBE	GEL	35.4	4
52000-072-02	Muscle Rub Pain Reliever Gel	1 in 1 CARTON	GEL	1	4
52000-072-03	Muscle Rub Pain Reliever Gel	35.4 g in 1 TUBE	GEL	35.4	3
52000-072-04	Muscle Rub Pain Reliever Gel	1 in 1 CARTON	GEL	1	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-072	MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC]	4	Current NDC, Legacy NDC, 2 package rows	20241212_b9a563b6-7988-79df-e053-2995a90a752b.zip
52000-072	MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC]	2	Current NDC, Legacy NDC, 2 package rows	20241218_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 35 of 241 · 4,814 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
KT Pain Relief Cream Magnesium with Cooling 5% Menthol	KT PAIN RELIEF CREAM MAGNESIUM WITH COOLING 5% MENTHOL	Clarion Brands LLC	4fe64056-f3c6-bc76-e063-6294a90a7e62	2026-04-20	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
4x Medicated Toothache and Gum Cream	BENZOCAINE	CVS	a7576238-e7c8-7e86-e053-2995a90aaeb5	2026-04-20	Warnings	Exact identifier unii: L7T10EIP3A
Lidothol ES Patch	LIDOTHOL ES PATCH	Direct_Rx	4fe72fca-9689-fff4-e063-6394a90a3ad2	2026-04-20	Warnings, Adverse reactions	Exact identifier unii: L7T10EIP3A
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 unii: L7T10EIP3A
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	9f991292-bbaa-4f4e-b2cb-059d1a04849e	2026-04-20	Warnings	Exact identifier unii: L7T10EIP3A
Sting Relief Swab	BENZOCAINE	4 Visions LLC	4fc7a356-2f1d-85af-e063-6394a90aec6b	2026-04-18	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
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 unii: L7T10EIP3A
LidoPro	LIDOCAINE AND MENTHOL	Advanced Rx of Tennessee, LLC	4faa515f-6040-d948-e063-6294a90a187f	2026-04-17	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
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 unii: 5TJD82A1ET
Ice Gel ICE COLD ANALGESIC	MENTHOL	Universal Distribution Center LLC	4f921ced-7722-cba5-e063-6294a90a650b	2026-04-16	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
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 unii: L7T10EIP3A
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 unii: 5TJD82A1ET
Tartar control plus	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	H E B	e425bc4c-88c7-48ec-98ef-46b45436a689	2026-04-16	Warnings, Adverse reactions	Exact identifier unii: L7T10EIP3A
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 unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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