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 21 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
New Terocin	METHYL SALICYLATE, CAPSAICIN, AND MENTHOL	ASCLEMED USA INC.	68dc0231-3364-448b-bde9-f19fa122c765	2026-05-05	Warnings	Exact identifier application number: M017
Lidocaine 4% Patch	LIDOCAINE 4%	SOLA Pharmaceuticals	c31957dd-edea-ce98-e053-2a95a90a9c2d	2026-05-05	Warnings	Exact identifier application number: M017
Biofreeze Triple Target Gel	CAMPHOR, CAPSAICIN, MENTHOL	Reckitt Benckiser LLC	511852c8-7428-3234-e063-6394a90a5bc2	2026-05-05	Warnings	Exact identifier application number: M017
5Kind DMSO Pain Relieving	CAMPHOR (SYNTHETIC)	5Kind Trading LTD	62b55114-47f4-473a-8406-78238c3c1fa2	2026-05-04	Warnings	Exact identifier application number: M017
Zinc Oxide with Menthol and White Petrolatum	MENTHOL, ZINC OXIDE, WHITE PETROLATUM	Aldermed Inc.	f993fc0a-bd80-4345-a948-65ac03f910e2	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE PRODUCTS BURN RELIEF	LIDOCAINE HYDROCHLORIDE	EVERLIT GLOBAL INC.	d7ec5720-4d1f-4943-ae36-c7d6acbae7d7	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE PRODUCTS BURN RELIEF	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	5371dae4-ea63-46cc-ac26-5418f359c63e	2026-05-04	Warnings	Exact identifier application number: M017
EVERLIT CARE BURN	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	a2cf1726-3dc9-4624-b898-ac91fb4cbdb2	2026-05-04	Warnings	Exact identifier application number: M017
FIRSTAR BURN	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	186343c5-2e71-49c4-8d64-5fb3131239fa	2026-05-04	Warnings	Exact identifier application number: M017
Feminine Anti Itch Cream	BENZOCAINE,RESORCINOL	TRIFECTA PHARMACEUTICALS USA LLC	50c3acbf-b873-908a-e063-6294a90a66b7	2026-05-01	Warnings	Exact identifier application number: M017
24 7 Relief and Recovery Pain Relieving	MENTHOL, UNSPECIFIED FORM	Triplicare Inc	53ca807b-3ec2-4b5e-aa5a-6dcb756bb423	2026-04-30	Warnings	Exact identifier application number: M017
FIRST AID BURN	LIDOCAINE HYDROCHLORIDE,BENZALKONIUM CHLORIDE	4 Visions LLC	50b1351d-72dd-e0c9-e063-6294a90ac743	2026-04-30	Warnings	Exact identifier application number: M017
TheraCare Flexible Pain Relieving	LIDOCAINE	Veridian Healthcare	4f108002-2cae-0671-e063-6294a90ab6cf	2026-04-30	Warnings	Exact identifier application number: M017
Pain Relief Gel Roll On	MENTHOL	Trifecta Pharmaceuticals USA	50b1a420-d5cd-6d61-e063-6294a90a0451	2026-04-30	Warnings	Exact identifier application number: M017
Dr. Numb	LIDOCAINE AND BENZETHONIUM CHLORIDE CREAM	Shinpharma Inc	d8cdccdb-775b-4970-a6ea-50b62df221d6	2026-04-30	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	Padagis Israel Pharmaceuticals Ltd	2dc7f76f-f9ad-46ba-8b41-952e1c15f052	2026-04-29	Warnings	Exact identifier application number: M017
anti itch	HYDROCORTISONE	HyVee Inc	e1db3641-2e83-4fec-8394-98d0d876ce0d	2026-04-29	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Roll On	MENTHOL, METHYL SALICYLATE	PT. EAGLE INDO PHARMA	50805eee-33b3-86bd-e063-6294a90a77d8	2026-04-28	Warnings	Exact identifier application number: M017
FixMySkin Healing Balm Vanilla Flavor	HYDROCORTISONE	Lovely Skin, Inc.	52f7a561-a0b5-4562-a588-d74fd874b83a	2026-04-28	Warnings	Exact identifier application number: M017
Blue Star Medicated	CAMPHOR	Focus Consumer Healthcare, LLC	56df008e-a23b-4870-e054-00144ff8d46c	2026-04-27	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