Home NDC 83781-006 MQ Pain Relieving Patch
Product NDC 83781-006
11-digit product format 837810006
Labeler code 83781
Product ID 83781-006_3113d5b9-c963-4cbb-e063-6294a90a9188
Type HUMAN OTC DRUG
Nonproprietary name Pain Relieving Patch
Dosage form PATCH
Route TOPICAL
Labeler Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-05
Substance LEVOMENTHOL; METHYL SALICYLATE; CAMPHOR (SYNTHETIC); .ALPHA.-TOCOPHEROL ACETATE
Active strength 5.7; 6.3; 1.2; 2 g/1001; g/1001; g/1001; g/1001
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 · 28 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 83781-006-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 83781-006-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 83781-006-03 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 83781-006-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 83781-006-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 83781-006-03 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 83781-006-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 83781-006-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 83781-006-03 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 83781-006-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 83781-006-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 83781-006-03 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 83781-006-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 83781-006-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 83781-006-03 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 83781-006-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 83781-006-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 83781-006-03 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 83781-006-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 83781-006-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 83781-006-03 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 MQ Pain Relieving Patch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEVOMENTHOL 5.7 g/1001 METHYL SALICYLATE 6.3 g/1001 CAMPHOR (SYNTHETIC) 1.2 g/1001 .ALPHA.-TOCOPHEROL ACETATE 2 g/1001
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 83781-006-01 MQ Pain Relieving Patch 30 in 1 BOX PATCH 30 2 83781-006-02 MQ Pain Relieving Patch 60 in 1 BOX PATCH 60 2 83781-006-03 MQ Pain Relieving Patch 240 in 1 BOX PATCH 240 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83781-006 MQ PAIN RELIEVING PATCH (PAIN RELIEVING PATCH) PATCH [ZHENGZHOU MIAOQI PHARMACEUTICAL TECHNOLOGY CO., LTD] 2 Current NDC, 3 package rows 20250326_0978ff22-c357-e266-e063-6394a90a98a4.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 104 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lidocare Arm, Neck, Leg 4% LIDOCAINE Kingsway Pharmaceuticals dba NFI, LLC 59a104ee-7034-99c3-e053-2991aa0a164c 2025-01-06 Warnings Exact identifier application number: M017 Salonpas LIDOCAINE Pain Relieving LIDOCAINE Hisamitsu Pharmaceutical Co., Inc. 4f3a438c-f378-4d2a-a95c-58e56cf1e797 2025-01-06 Warnings Exact identifier application number: M017 Lidocare 03 4% LIDOCAINE Kingsway Pharmaceuticals dba NFI, LLC 416ebf5a-2efb-6d0b-e054-00144ff88e88 2025-01-06 Warnings Exact identifier application number: M017 AVCOO Pain Relief Roll-on MENTHOL ADP Health Limited e0bb77b2-45ee-45fa-9659-9c7d99bb20dc 2025-01-05 Warnings Exact identifier application number: M017 health and beyond BURN LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE Nantong Health & Beyond Hygienic Products Inc. 0b6bb3ed-50fb-40c4-acb6-ae3f16031531 2025-01-05 Warnings Exact identifier application number: M017 glo SKIN BEAUTY Remedy Gel GLO SKIN BEAUTY REMEDY GEL Hayden Caleel LLC aa47ff08-07b3-4fd1-bae5-420e4b928f06 2025-01-05 Warnings Exact identifier application number: M017 Capsaicin 0.025% Cream CAPSAICIN 0.025% Puretek Corporation 28f00df0-c416-f17b-e063-6294a90a5570 2025-01-02 Warnings Exact identifier application number: M017 AVON HeXashield Pain Relief for Muscle, Back and Joint Cream CAMPHOR, MENTHOL, METHYL SALICYLATE Tai Guk Pharm. Co., Ltd. 8f29ffd7-48b9-109f-e053-2995a90ab215 2025-01-01 Warnings Exact identifier application number: M017 AVON HeXashield Arthritis Pain Relief Cream Capsaisin CAPSAISIN Tai Guk Pharm. Co., Ltd. 8f286a9d-8765-21b3-e053-2a95a90ae43a 2025-01-01 Warnings Exact identifier application number: M017 AVON HeXashield Anti Itch Cream with Healing Aloe HYDROCORTISONE Tai Guk Pharm. Co., Ltd. 8f2aa11d-d794-6f3e-e053-2995a90a1d9d 2025-01-01 Warnings Exact identifier application number: M017 HeXashield Anti Itch Cream with Healing Aloe HYDROCORTISONE Tai Guk Pharm. Co., Ltd. b9d033f3-4d12-a2c8-e053-2995a90ac7f1 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Pain Relief with Menthol MENTHOL Green Compass, Inc. 0a0c212e-ae5d-8505-e063-6394a90af622 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Pain Relief CAMPHOR, MENTHOL, METHYL SALICYLATE Green Compass, Inc. 0a0b688e-50f1-3eb1-e063-6394a90a7efa 2025-01-01 Warnings Exact identifier application number: M017 Green Compass Reduce Topical Pain CAMPHOR, MENTHOL, METHYL SALICYLATE Green Compass, Inc. 8cb80362-5d24-1ee3-e053-2a95a90afcdf 2025-01-01 Warnings Exact identifier application number: M017 OKeeffes Working Hands Pain Relief Skin Protectant ALLANTOIN, LIDOCAINE HYDROCHLORIDE The Gorilla Glue Company/O'Keeffe's Company 0685da25-c9fa-e1cd-e063-6394a90ae1b3 2025-01-01 Warnings Exact identifier application number: M017 Icy Hot with Lidocaine Pain Relieving LIDOCAINE HCL AND MENTHOL Chattem, Inc. 75b28b06-77ea-4fea-b516-2e8a0dac7037 2025-01-01 Warnings Exact identifier application number: M017 Advanced Seal Barrier plus Pain Relief LIDOCAINE Kericure Inc. 7ac95325-e6e9-4c56-9315-876c00af7c98 2025-01-01 Warnings Exact identifier application number: M017 FixMySkin Healing Balm Fragrance-Free HYDROCORTISONE Lovely Skin, Inc. c12af4c6-2f05-46ec-b901-1a4fcd750180 2024-12-31 Warnings Exact identifier application number: M017 Pain Relieving Cream Lidocaine BENZYL ALCOHOL, LIDOCAINE HCI Trifecta Pharmaceuticals USA LLC 039a2036-54b2-cf28-e063-6294a90a8ce6 2024-12-31 Warnings Exact identifier application number: M017 Cold Therapy Pain Relief Walgreens MENTHOL 10.5% WALGREEN COMPANY f1daa68d-1b12-c28a-e053-2995a90a0949 2024-12-31 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 83781-006-01 83781000601 30 PATCH in 1 BOX (83781-006-01) 30 patch 2023-11-05 No No Current 83781-006-02 83781000602 60 PATCH in 1 BOX (83781-006-02) 60 patch 2023-11-05 No No Current 83781-006-03 83781000603 240 PATCH in 1 BOX (83781-006-03) 240 patch 2023-11-05 No No Current