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: 2026-10-21
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	2026-10-21	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 95 of 238 · 4,757 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
The Pharma-C Company 70 Isopropyl Alcohol Pads	ISOPROPYL ALCOHOL	Kleen Test Products Corporation	c5df867b-1b8d-4e38-8c32-7d528b982590	2025-12-09	Warnings	Exact identifier unii: ND2M416302
Vaporizing Rub	CAMPHOR, EUCALYPTUS OIL AND MENTHOL	ALAINA HEALTHCARE PRIVATE LIMITED	4c6a7ac0-be76-42b0-9a08-b287e70a3460	2025-12-09	Warnings	Exact identifier unii: L7T10EIP3A unii: 5TJD82A1ET
Pain Relief Balm	MENTHOL AND CAMPHOR	ALAINA HEALTHCARE PRIVATE LIMITED	12d76b8f-4b1d-4f2d-9722-0adb55093cc4	2025-12-09	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET
Firstep Firstflush	EYEWASH	Encon Safety Products, Inc.	a44beb26-79ae-98bd-e053-2995a90a9b74	2025-12-09	Warnings	Exact identifier unii: 059QF0KO0R
Trojan Extended Pleasure	BENZOCAINE	Church & Dwight Co., Inc.	be731682-4174-649a-e053-2a95a90a3987	2025-12-09	Warnings	Exact identifier application number: M017
Walgreens Childrens Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Walgreen Company	327a7226-84b9-26d7-e063-6394a90a99b9	2025-12-09	Warnings	Exact identifier unii: L7T10EIP3A
Stopain Clinical Continuous	MENTHOL	Troy Manufacturing, Inc.	65f8d212-0f0e-4893-b6af-bd68bba46443	2025-12-09	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
Pain and Itch Relief 4% Lidocaine	LIDOCAINE	Walgreens	f84e76a9-6af6-4fd1-be4e-efa05728cbfd	2025-12-09	Warnings	Exact identifier application number: M017
Capsimide	CAPSAICIN 0.025% TOPICAL PATCH	Sola Pharmaceuticals	e81c2de8-6429-d681-e053-2995a90a36a9	2025-12-08	Warnings	Exact identifier application number: M017
Extra Strength Cold-Hot Medicated Patches	MENTHOL	Cardinal Health, 110 dba LEADER	a2895c03-747c-4220-8052-4f0428062622	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
Leader PAIN RELIEF PATCHES	LIDOCAINE	Cardinal Health, 110 dba LEADER	5feae39e-3ab8-4cda-b9e8-dc221aea2417	2025-12-08	Warnings	Exact identifier application number: M017
Pain Relief Patches	CAMPHOR, MENTHOL, METHYL SALICYLATE	Cardinal Health, 110 dba LEADER	f8837b69-8d85-448c-a4b4-be911bca1f6c	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET
CAPSAICIN HOT PATCHES	CAPSAICIN	Cardinal Health, 110 dba LEADER	76e6bc39-643c-4264-8d98-0e4fa7d778e2	2025-12-08	Warnings	Exact identifier application number: M017
Leader PAIN RELIEF PATCHES	LIDOCAINE	Cardinal Health, 110 dba LEADER	3be6defd-f429-4dc7-8b37-5910705c0b81	2025-12-08	Warnings	Exact identifier application number: M017
LenzaPro Flex	LIDOCAINE/MENTHOL	SOLA Pharmaceuticals	ba498f1d-460b-f4e6-e053-2995a90a5755	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
LidaFlex	LIDOCAINE	SOLA Pharmaceuticals	b9e49529-13b4-1b0b-e053-2995a90adc7a	2025-12-08	Warnings	Exact identifier application number: M017
Rugby Menthol Hot Cold Patch	MENTHOL	RUGBY LABORATORIES	c68d29c2-9b56-4994-e053-2a95a90ae60e	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
Neuracin Topical Gel	NEURACIN TOPICAL ANALGESIC GEL	SOLA Pharmaceuticals	c3166926-30c2-2128-e053-2a95a90a0bf2	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET
Triceptin	LIDOCAINE / MENTHOL / METHYL SALICYLATE	SOLA Pharmaceuticals	ef1b98ab-d2db-038c-e053-2995a90a94b4	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A
SynoFlex Patch	SYNOFLEX PATCH	Sola Pharmaceuticals	de2042c4-6c5e-7365-e053-2a95a90ada2a	2025-12-08	Warnings	Exact identifier application number: M017 unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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