MQ Pain Relieving Patch
83781-006 Update V2
Approved
Approval ID
0978ff22-c357-e266-e063-6394a90a98a4
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Mar 24, 2025
Manufacturers
FDA
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
DUNS: 701762807
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Pain Relieving Patch
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code83781-006
Application NumberM017
Product Classification
M
Marketing Category
C200263
G
Generic Name
Pain Relieving Patch
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 24, 2025
FDA Product Classification
INGREDIENTS (9)
PANAX NOTOGINSENG ROOTInactive
Code: GQX1C1175U
Classification: IACT
LEVOMENTHOLActive
Quantity: 5.7 g in 100 1
Code: BZ1R15MTK7
Classification: ACTIB
METHYL SALICYLATEActive
Quantity: 6.3 g in 100 1
Code: LAV5U5022Y
Classification: ACTIB
GYNOSTEMMA PENTAPHYLLUM LEAFInactive
Code: 5DWS84R85M
Classification: IACT
CAMPHOR (SYNTHETIC)Active
Quantity: 1.2 g in 100 1
Code: 5TJD82A1ET
Classification: ACTIB
FLEMINGIA PROSTRATA WHOLEInactive
Code: R0GG9QUA0Q
Classification: IACT
CINNAMON OILInactive
Code: E5GY4I6YCZ
Classification: IACT
CLOVEInactive
Code: K48IKT5321
Classification: IACT
.ALPHA.-TOCOPHEROL ACETATEActive
Quantity: 2 g in 100 1
Code: 9E8X80D2L0
Classification: ACTIB