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 88 of 238 · 4,757 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.