Home NDC 52000-072 Muscle Rub Pain Reliever Gel
Product NDC 52000-072
11-digit product format 520000072
Labeler code 52000
Product ID 52000-072_db1541b7-b2be-4751-a391-f0966f834ca3
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route TOPICAL
Labeler Universal Distribution Centre LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-24
Substance MENTHOL, UNSPECIFIED FORM
Active strength 25 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 52000-072-02 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 52000-072-02 f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Muscle Rub Pain Reliever Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 25 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 282805 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# 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 48 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52000-072-01 52000007201 35.4 g in 1 TUBE 35.4 g Historical 52000-072-02 52000007202 1 TUBE in 1 CARTON (52000-072-02) > 35.4 g in 1 TUBE (52000-072-01) 1 tube 2021-01-24 0000-00-00 No No Current 52000-072-03 52000007203 35.4 g in 1 TUBE 35.4 g Historical 52000-072-04 52000007204 1 TUBE in 1 CARTON (52000-072-04) / 35.4 g in 1 TUBE (52000-072-03) 1 tube 2021-01-24 No No Current