Home NDC 76348-511 MAG 5 PT WARMING FORMULA
Product NDC 76348-511
11-digit product format 763480511
Labeler code 76348
Product ID 76348-511_574988ea-50c0-bcb0-e063-6294a90ad749
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form CREAM
Route TOPICAL
Labeler RENU LABORATORIES, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-19
Substance MENTHOL
Active strength 5.6 g/112g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 76348-511-05 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 76348-511-05 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 76348-511-05 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 76348-511-05 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76348-511-05 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76348-511-05 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76348-511-05 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 MAG 5 PT WARMING FORMULA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 5.6 g/112g
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 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 76348-511-04 MAG 5 PT WARMING FORMULA 112 g in 1 JAR CREAM 112 10 76348-511-05 MAG 5 PT WARMING FORMULA 1 in 1 BOX CREAM 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76348-511 MAG 5 PT WARMING FORMULA (MENTHOL) CREAM [RENU LABORATORIES, LLC] 9 Current NDC, 2 package rows 20250330_a499ac9b-0e8e-e23f-e053-2a95a90abe9a.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 38 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TheraCare Muscle and Joint Gel Vanishing Scent MENTHOL 2.5% Veridian Healthcare 494d2a85-45a8-12a2-e063-6294a90a391b 2026-01-26 Warnings Exact identifier application number: M017 Lidocaine Pain Relief LIDOCAINE Trifecta Pharmaceuticals USA, LLC. 493c09d0-16d7-7413-e063-6394a90aa052 2026-01-26 Warnings Exact identifier application number: M017 Topcare Medicated Pain Relieving Patch 60ct TOPCARE PAIN RELIEF PATCH EXTRA STRENGTH Topco Associates LLC 4953c12b-ca6d-d21e-e063-6294a90ac990 2026-01-26 Warnings Exact identifier application number: M017 Dr Sabharwals MENTHOL 5% PATCH Dr. Sabharwal's Wound Care 1025b986-a1e5-701d-e063-6294a90a33fd 2026-01-24 Warnings Exact identifier application number: M017 Target Up and Up Pain Relief Menthol Topical Analgesic MENTHOL Target Corporation 4910f32f-c639-0215-e063-6394a90a1c7b 2026-01-23 Warnings Exact identifier application number: M017 Rapidol HYDROCORTISONE Pharmadel LLC 19a1f1e2-bc6b-7153-e063-6294a90ab115 2026-01-23 Warnings Exact identifier application number: M017 CVS 9083 Maximum Strength Lidocaine 4 Pain Relief Patch 1ct Large LIDOCAINE CVS PHARMACY, INC 4914965f-1164-e20e-e063-6294a90ac221 2026-01-23 Warnings Exact identifier application number: M017 THE GOO MEDICATED PAIN RELIEF METHYL SALICYLATE, MENTHOL, CAMPHOR APSM PERFORMANCE, LLC db4c321c-8cdc-5a11-e053-2995a90a91a1 2026-01-23 Warnings Exact identifier application number: M017 Dr Sabharwals LIDOCAINE 4% AND MENTHOL 1% PATCH Dr. Sabharwal's Wound Care 10249d0f-5ee1-6892-e063-6394a90a967e 2026-01-23 Warnings Exact identifier application number: M017 Easment DMSO cream MENTHOL 1.00% Easment LLC 48f5544e-1cfd-864a-e063-6394a90a71f1 2026-01-22 Warnings Exact identifier application number: M017 Aveeno 1% Hydrocortisone Anti-Itch Cream HYDROCORTISONE Kenvue Brands LLC 1ac0ac4e-af76-9a3e-e063-6394a90a1269 2026-01-22 Warnings Exact identifier application number: M017 RAYO ACTIVE ICE MENTHOL, CAMPHOR Quimicas Handal de Centroamerica SA de CV 09e4a36b-020a-c5b1-e063-6394a90a3e31 2026-01-22 Warnings Exact identifier application number: M017 X-Treme Freeze COLD THERAPY GEL Dynarex Corporation 79f0802f-03ad-bf8f-e053-2991aa0ae4b5 2026-01-22 Warnings Exact identifier application number: M017 Anti Itch HYDROCORTISONE HyVee Inc ae31f1f5-db70-45cf-850e-67bfe6860748 2026-01-21 Warnings Exact identifier application number: M017 ULTRA RELIEF MENTHOL, CAMPHOR CHEMCO CORPORATION 48ea80cf-af54-ce5f-e063-6394a90ac493 2026-01-21 Warnings Exact identifier application number: M017 Healthy Back Institute Rub On Relief ANALGESIC Eagle Labs Inc. 17dff3c1-3c0b-16f6-e063-6394a90a3c05 2026-01-21 Warnings Exact identifier application number: M017 Pain Relief ANALGESIC Fullstack Fulfillment 2a433cee-8b6f-c280-e063-6394a90ae25a 2026-01-21 Exact identifier application number: M017 Walgreens Anti Itch Cream ANTI ITCH CREAM Walgreens Company b545553a-283a-48af-adc5-763758a9ff24 2026-01-21 Warnings Exact identifier application number: M017 CVS Health Maximum Strength Lidocaine Pain Relief Cream Plus Menthol LIDOCAINE HCL, MENTHOL CVS Pharmacy 8aaffa3f-f82f-470c-902d-f366f1a66305 2026-01-21 Warnings Exact identifier application number: M017 LIGHTS Instant Sting Relief Pad BENZOCAINE Lights Medical Manufacture Co., Ltd. 28dd82a7-f360-a022-e063-6394a90a3a76 2026-01-21 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76348-511-04 76348051104 112 g in 1 JAR 112 g Historical 76348-511-05 76348051105 1 JAR in 1 BOX (76348-511-05) / 112 g in 1 JAR (76348-511-04) 1 jar 2019-03-19 No No Current