Home NDC 52000-072-01 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 FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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 102 of 237 · 4,734 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC fc8a8f20-97ab-481e-e053-6394a90a3525 2025-11-20 Warnings Exact identifier application number: M017 unii: L7T10EIP3A FOOT PAIN RELIEF ROLL-ON LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 43edcea0-ab04-f368-e063-6294a90a817a 2025-11-19 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Absolut Skin Corticosoothe Anti-Itch HYDROCORTISONE Absolut Skin Incorporated deb52218-9176-4aaa-a22f-b66dada6690f 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 43f3d189-f6b7-02ed-e063-6394a90afd73 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch HealthA2Z LIDOCAINE InterMed Laboratories Private Limited 43f3e288-e828-8130-e063-6394a90a6d44 2025-11-19 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Leader LIDOCAINE InterMed Laboratories Private Limited 42f06914-c8b8-ea9c-e063-6294a90a79e6 2025-11-19 Warnings Exact identifier application number: M017 Dukal Alcohol Prep Pad ISOPROPYL ALCOHOL Dukal LLC 953b0dd6-a667-4146-815e-6845aba0309b 2025-11-19 Warnings Exact identifier unii: ND2M416302 Dukal Sterile Alcohol Swabstick ISOPROPYL ALCOHOL Dukal LLC 8e47e9ad-cea4-76a4-e053-2a95a90ae780 2025-11-19 Warnings Exact identifier unii: ND2M416302 CVS Anti-Itch CAMPHOR, MENTHOL CVS 87715662-c788-9a8d-e053-2a95a90acb53 2025-11-19 Warnings Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET Walgreen Anti Itch CAMPHOR, MENTHOL Walgreens b4f47a8d-d4a6-9233-e053-2a95a90afd90 2025-11-19 Warnings Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET Leader Anti-Itch CAMPHOR, MENTHOL LEADER/Cardinal Helath 110, Inc. 9ca985c6-5017-0558-e053-2995a90a8202 2025-11-19 Warnings Exact identifier application number: M017 unii: L7T10EIP3A unii: 5TJD82A1ET CVS Anti-Itch PRAMOXINE HCL CVS 87fc476a-5b12-7383-e053-2995a90a530b 2025-11-19 Warnings Exact identifier application number: M017 Walgreen Anti-Itch PRAMOXINE HCL Walgreens b5f9d1c5-891e-4377-e053-2995a90aa281 2025-11-19 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET PAIN RELIEF 89f5f688-856f-f2df-e053-2995a90a73cf 2025-11-19 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Itch Eraser DIPHENHYDRAMINE HCL Tender Corporation d/b/a Adventure Ready Brands 2204e135-6a23-68a2-e063-6394a90ac019 2025-11-18 Warnings Exact identifier application number: M017 Analgesic Balm MENTHOL 10%, METHYL SALICYLATE 15% Geri-Care Pharmaceuticals, Corp c8594e10-661f-6ff3-e053-2995a90ab4fc 2025-11-18 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Mag 5 PT Cooling Formula Recovery Cream MENTHOL RENU LABORATORIES, LLC a45cde67-64ec-643b-e053-2a95a90a10b6 2025-11-18 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Sterile Water WATER Fresenius Kabi USA, LLC fd823bef-c14c-4708-a18a-8aaa8470412f 2025-11-18 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Quality Choice Medicated Chest Rub CAMPHOR, MENTHOL, EUCALYPTUS OIL QUALITY CHOICE (Chain Drug Marketing Association) c0e3c959-bed6-2ce5-e053-2995a90a0be9 2025-11-17 Warnings Exact identifier unii: L7T10EIP3A unii: 5TJD82A1ET After Ivy Wipe CAMPHOR Tender Corporation d/b/a Adventure Ready Brands 21d98018-826a-1d0d-e063-6294a90a0a71 2025-11-17 Warnings Exact identifier application number: M017 unii: 5TJD82A1ET
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.