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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
BZ1R15MTK7	Internal UNII lookup
LAV5U5022Y	Internal UNII lookup
5TJD82A1ET	Internal UNII lookup
9E8X80D2L0	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0978ff22-c357-e266-e063-6394a90a98a4	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
83781-006-01	2025-03-24	83781-006 Update V2
83781-006-02	2025-03-24	83781-006 Update V2
83781-006-03	2025-03-24	83781-006 Update V2
83781-006-01	2025-01-30	83781-006 Update V2
83781-006-02	2025-01-30	83781-006 Update V2
83781-006-03	2025-01-30	83781-006 Update V2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	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 5 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
RELIBONEOintment	TOPICAL ANALGESICOINTMENT	Guangdong Jiaoyu Biotechnology Co., Ltd	58ddaaf6-18ec-8c5b-e063-6294a90a2828	2026-08-12	Warnings	Exact identifier application number: M017
Capsaicin Cream	CAPSAICIN	Trifecta Pharmaceuticals USA LLC	58de3a29-2bec-6e44-e063-6394a90a9c1a	2026-08-12	Warnings	Exact identifier application number: M017
HYDROCORTISONE	HYDROCORTISONE	Amazon.com Services LLC	f40b4223-e81f-4cd0-bc9b-d3d33ce8cce5	2026-08-12	Warnings	Exact identifier application number: M017
Muscle Rub Cream	MUSCLE RUB	ALLIED TRADE LINK LLC	11d33e60-8c64-4316-a29a-d17e3e6e4a28	2026-08-11	Warnings	Exact identifier application number: M017
Gee Gason	MALE GENITAL DESENSITIZER	Mon Gars Boutique Inc	58c75e5c-b801-017f-e063-6394a90a1c75	2026-08-11	Warnings	Exact identifier application number: M017
Capsaicin Cream	CAPSAICIN	Trifecta Pharmaceuticals USA LLC	58c84330-15bf-c397-e063-6394a90aba05	2026-08-11	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	TARGET Corporation	4a140b9a-0e3c-4b50-b9c0-9e72616bb7d5	2026-08-11	Warnings	Exact identifier application number: M017
Itch Relief	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	CVS Pharmacy	0e988da1-1904-431d-a152-bdb2aacc8e16	2026-08-11	Warnings	Exact identifier application number: M017
Medicated BODY	MENTHOL	CVS Pharmacy, Inc.	a0f61498-69c8-4ce0-bbd7-3a807f192d36	2026-08-11	Warnings	Exact identifier application number: M017
Muscle Move	MENTHOL	Saje Natural Wellness Inc.	526d3305-4cf8-2fc5-e063-6394a90ad53b	2026-08-10	Warnings	Exact identifier application number: M017
Relieve and Relax Pain Relieving	CAMPHOR (SYNTHETIC), MENTHOL	MAC Innovations, LLC	c0528c36-d322-8110-e053-2995a90add6c	2026-08-08	Warnings	Exact identifier application number: M017
CVS Pain Relief	MENTHOL	CVS Pharmacy	4aa629f5-8b8f-cc67-e063-6394a90a019f	2026-08-07	Warnings	Exact identifier application number: M017
Instant Cooling Itch Relief	HYDROCORTISONE	CVS Pharmacy	46545d04-5958-d136-e063-6394a90a3462	2026-08-07	Warnings	Exact identifier application number: M017
CVS Itch Relief	PRAMOXINE HYDROCHLORIDE, ZINC ACETATE	CVS Pharmacy	46921bea-fcbe-94d6-e063-6394a90a726b	2026-08-07	Warnings	Exact identifier application number: M017
CVS Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	CVS Pharmacy	524605f9-8b04-b600-e063-6394a90a4a02	2026-08-07	Warnings	Exact identifier application number: M017
Lidonex	LIDOCAINE HCL, MENTHOL	Aldama Pharmaceuticals, Inc	365cf19c-70e0-c4e9-e063-6294a90ac428	2026-08-07	Warnings	Exact identifier application number: M017
Blaster Pain Relief Stick	MENTHOL, METHYL SALICYLATE, CAMPHOR	Kalahari Rose, LLC	587d660a-5f80-de5a-e063-6394a90aa287	2026-08-07	Warnings	Exact identifier application number: M017
Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Cardinal Health, 110 dba Leader	3ed7b8a1-012f-459d-878c-813b93d4673c	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Gel Cooling Pain Relief	MENTHOL	The Kroger Co.	6fb0acc8-8dab-452c-b09e-de97306e1c32	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Lidocaine Tattoo Wipe	LIDOCAINE HYDROCHLORIDE	MD Tattoo Company	369c1d16-597c-e1dc-e063-6394a90a3104	2026-08-06	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
BZ1R15MTK7	LEVOMENTHOL	2216-51-5	LEVOMENTHOL
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)
9E8X80D2L0	.ALPHA.-TOCOPHEROL ACETATE	7695-91-2	.ALPHA.-TOCOPHEROL ACETATE

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
83781-006 Update V2	Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	2025-03-24	HUMAN OTC DRUG LABEL	2