Mqupin Knee Patch

Product NDC: 83781-002
11-digit product format: 837810002
Labeler code: 83781
Product ID: 83781-002_349c91e3-026f-ba51-e063-6394a90a3fa3
Type: HUMAN OTC DRUG
Nonproprietary name: Knee 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: CAMPHOR (SYNTHETIC); BORNEOL
Active strength: 1.5; 1.2 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 · 21 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	83781-002-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	83781-002-02	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	83781-002-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	83781-002-02	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	83781-002-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	83781-002-02	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	83781-002-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	83781-002-02	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	83781-002-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	83781-002-01	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	83781-002-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	83781-002-01	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	83781-002-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	83781-002-01	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: Mqupin Knee Patch
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	1.5 g/1001
BORNEOL	1.2 g/1001

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup
M89NIB437X	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
09772e4b-8193-3771-e063-6394a90a9516	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
83781-002-01	2025-03-24	83781-002 Update V3 Update Pack
83781-002-02	2025-03-24	83781-002 Update V3 Update Pack
83781-002-01	2025-01-30	83781-002 Update V3 Update Pack
83781-002-02	2025-01-30	83781-002 Update V3 Update Pack

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
83781-002-01	Mqupin Knee Patch	14 in 1 BOX	PATCH	14	3
83781-002-02	Mqupin Knee Patch	28 in 1 BOX	PATCH	28	3
83781-002-03	Mqupin Knee Patch	42 in 1 BOX	PATCH	42	3
83781-002-04	Mqupin Knee Patch	64 in 1 BOX	PATCH	64	3
83781-002-05	Mqupin Knee Patch	100 in 1 BOX	PATCH	100	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83781-002	MQUPIN KNEE PATCH (KNEE PATCH) PATCH [ZHENGZHOU MIAOQI PHARMACEUTICAL TECHNOLOGY CO., LTD]	3	Current NDC, 5 package rows	20250509_09772e4b-8193-3771-e063-6394a90a9516.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 24 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
A Health Itch Relief Gel	ITCH RELIEF GEL	Pharma Nobis, LLC	4f80c403-c760-31ec-e063-6394a90a61c9	2026-04-15	Warnings	Exact identifier application number: M017
Family Care Antibiotic Pain Relief 0.33oz	ANTIBIOTIC PAIN RELIEF	United Exchange Corp	4f8405fc-3e38-05d9-e063-6394a90a4cda	2026-04-15	Warnings	Exact identifier application number: M017
BiteMD	INSECT BITE RELIEF	Wisconsin Pharmacal Company	4f860c1e-a638-4923-e063-6294a90ae7e2	2026-04-15	Warnings	Exact identifier application number: M017
LavaDerm AfterSun	MENTHOL	Young Living Essential Oils, LC.	4fcddcf1-36db-2f1a-e054-00144ff8d46c	2026-04-15	Warnings	Exact identifier application number: M017
Arlun Numbing Cream	NUMBING CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	4f8b60f9-03e3-e731-e063-6294a90a3b0a	2026-04-15	Warnings	Exact identifier application number: M017
tuiwaro Numbing Cream	NUMBING CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	4f66178c-95d9-8c6a-e063-6294a90a2c09	2026-04-14	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Roll-On	LIDOCAINE 4%	Pharma Nobis, LLC	4f6d9a51-c42e-ca88-e063-6394a90a8659	2026-04-14	Warnings	Exact identifier application number: M017
Hot/Cold Menthol 16% Roll-On	HOT/COLD MENTHOL 16% ROLL-ON	Pharma Nobis, LLC	4f6f5a0b-3bfa-289e-e063-6294a90a94b3	2026-04-14	Warnings	Exact identifier application number: M017
Sting Relief Swab	BENZOCAINE	4 Visions LLC	4f76a8c5-fde6-eee0-e063-6394a90a09f8	2026-04-14	Warnings	Exact identifier application number: M017
Signature Pain Relief Cream	4% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	4f555b8f-5193-e685-e063-6294a90a7ba2	2026-04-13	Warnings	Exact identifier application number: M017
Deep Numbing Cream	MENTHOL	YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD	7943559b-de10-4214-96dc-f9cbac828f46	2026-04-13	Warnings	Exact identifier application number: M017
Hydrocortisone Cream 1%	HYDROCORTISONE CREAM 1% WITH ALOE	Publix Super Markets Inc.	3c45a654-7fec-55b3-e063-6294a90a184b	2026-04-13	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	AMERISOURCE BERGEN	4f5aea1c-ae51-4e1a-e063-6294a90a6aa1	2026-04-13	Warnings	Exact identifier application number: M017
ActivICE	MENTHOL	Medline Industries, LP	8465b443-abe9-78fb-e053-2a91aa0ac1d8	2026-04-13	Warnings	Exact identifier application number: M017
4Jointz	MENTHOL	ARP(USA) Pty Ltd	94a5b5f5-abf7-40b3-9dd7-43e2c22f138e	2026-04-13	Warnings	Exact identifier application number: M017
Sumifun Pain Relief Creams	METHYL SALICLATE CAPSAICIN CAMPHOR	Guchutang Biotechnology (Longyan) Co., Ltd	4f3dd96a-d843-d810-e063-6394a90a188e	2026-04-12	Warnings	Exact identifier application number: M017
BonicaEaseX 24 Hour Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co., Ltd.	17fc0cd1-710d-45e6-9513-d7100e3adb42	2026-04-10	Warnings	Exact identifier application number: M017
BonicaEaseX Colorless Roll-On Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co.,Ltd	acf460b4-1b41-4b30-a74a-6c3613119d8e	2026-04-10	Warnings	Exact identifier application number: M017
BonicaEaseX Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co.,Ltd	4d84b4fb-8f55-4b2b-b261-858edb7f3144	2026-04-10	Warnings	Exact identifier application number: M017
HealthWise Pain Relief Gel Patch	CAPSAICIN, MENTHOL	Veridian Healthcare	f5484151-b6da-4f64-867f-87160a4ec2d6	2026-04-10	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)
M89NIB437X	BORNEOL	507-70-0	BORNEOL

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83781-002-01	83781000201	14 PATCH in 1 BOX (83781-002-01)	14 patch	2023-11-05	No	No	Current
83781-002-02	83781000202	28 PATCH in 1 BOX (83781-002-02)	28 patch	2023-11-05	No	No	Current
83781-002-03	83781000203	42 PATCH in 1 BOX (83781-002-03)	42 patch	2023-11-05	No	No	Current
83781-002-04	83781000204	64 PATCH in 1 BOX (83781-002-04)	64 patch	2023-11-05	No	No	Current
83781-002-05	83781000205	100 PATCH in 1 BOX (83781-002-05)	100 patch	2023-11-05	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
83781-002 Update V3 Update Pack	Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	2025-05-08	HUMAN OTC DRUG LABEL	3