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 70 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aromalief Pain Relief Cream Orange Ginger	MENTHOL	Marketites LLC	9e8d3611-ef1b-4ac6-e053-2995a90af28a	2025-10-29	Warnings	Exact identifier application number: M017
Aromalief Calming Pain Relief Cream Lavender	MENTHOL	Marketites LLC	b8197d52-ccfb-b008-e053-2995a90a0a53	2025-10-29	Warnings	Exact identifier application number: M017
Aromalief Cozy Vanilla Pain Relief Cream	MENTHOL	Marketites LLC	3634e55e-8c62-a782-e063-6394a90a6508	2025-10-29	Warnings	Exact identifier application number: M017
BENOVA PAIN AND ITCH RELIEF	MENTHOL, 0.11%	BENOVA RX LLC	42513ee2-8b40-a9f3-e063-6394a90a9386	2025-10-29	Warnings	Exact identifier application number: M017
Burn Relief	LIDOCAINE	CVS Pharmacy	7e9285fd-26d5-3eac-e053-2991aa0ae2db	2025-10-29	Warnings	Exact identifier application number: M017
Coralite Ultra Strength Pain Relief	CAMPHOR MENTHOL	United Exchange Corp.	44ecf959-cc07-4adc-a500-075b2ee69548	2025-10-29	Warnings	Exact identifier application number: M017
GoodSense Pain Relief	LIDOCAINE	Geiss, Destin & Dunn, Inc	826f8da4-8468-ea0a-e053-2991aa0a66cb	2025-10-28	Warnings	Exact identifier application number: M017
CALMADOL	CAMPHOR, MENTHOL, METHYL SALICYLATE	GRANDALL DISTRIBUTING, LLC	31b7f84e-8b66-4d31-8e9c-279d0af2fe64	2025-10-28	Warnings	Exact identifier application number: M017
XRay DOL	CAMPHOR, MENTHOL, AND METHYL SALICYLATE	Genomma Lab USA, Inc.	e07fef46-68d9-769c-e053-2a95a90aa065	2025-10-28	Warnings	Exact identifier application number: M017
CVS Medicated Heat	CAPSICUM EXTRACT	CVS Pharmacy	81cd1019-93a6-311b-e053-2991aa0a7997	2025-10-28	Warnings	Exact identifier application number: M017
Foster and Thrive	LIDOCAINE	STRATEGIC SOURCING SERVICES, LLC	f950b072-d978-b629-e053-6394a90abfaf	2025-10-28	Warnings	Exact identifier application number: M017
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	Premier Brands of America, Inc.	d3452573-f91f-f157-e053-2a95a90a1ad8	2025-10-27	Warnings	Exact identifier application number: M017
PR	MENTHOL	Amphp, Inc	6f5b9e08-c445-4fac-e053-2a91aa0aa737	2025-10-27	Warnings	Exact identifier application number: M017
Lidocaine	BURN RELIEF	Foodhold USA	b25dc0df-02d0-41ac-b36c-2c04baa77ef2	2025-10-27	Warnings	Exact identifier application number: M017
Menthol	MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE	FSA Store Inc.	fb3548c8-f202-dc50-e053-6394a90a5b30	2025-10-27	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE CONTINUOUS SPRAY	Premier Brands of America, Inc.	d344f68b-9b62-3029-e053-2995a90a1665	2025-10-27	Warnings	Exact identifier application number: M017
Medi-First Hydrocortisone 1%	HYDROCORTISONE ACETATE 1%	Unifirst First Aid Corporation	f2b46d69-1c21-5ae9-e053-2a95a90a60a9	2025-10-24	Warnings	Exact identifier application number: M017
Extra Strength	MENTHOL AND METHYL SALICYLATE	Saje Natural Business Inc.	87d872b3-3231-d0f2-e053-2995a90a9d98	2025-10-24	Warnings	Exact identifier application number: M017
Coralite Muscle and Joint Pain Relief	CAMPHOR, MENTHOL, AND MEHTYL SALICYLATE	United Exchange Corporation	78edeeb8-3e3c-64bb-e053-2a91aa0a7bbc	2025-10-24	Warnings	Exact identifier application number: M017
Coralite Odor Free Pain Relief	LIDOCAINE	United Exchange Corporation	7966d9f2-22f9-a900-e053-2991aa0aba55	2025-10-24	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