Mqupin Knee Patch
83781-002 Update V3 Update Pack
Approved
Approval ID
09772e4b-8193-3771-e063-6394a90a9516
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.
Knee Patch
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code83781-002
Application NumberM017
Product Classification
M
Marketing Category
C200263
G
Generic Name
Knee Patch
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 24, 2025
FDA Product Classification
INGREDIENTS (9)
CINNAMONInactive
Code: 5S29HWU6QB
Classification: IACT
WORMWOODInactive
Code: F84709P2XV
Classification: IACT
SAFFRONInactive
Code: E849G4X5YJ
Classification: IACT
GINGERInactive
Code: C5529G5JPQ
Classification: IACT
CAMPHOR (SYNTHETIC)Active
Quantity: 1.5 g in 100 1
Code: 5TJD82A1ET
Classification: ACTIB
ARTEMISIA VULGARIS TOP OILInactive
Code: 72Q967Y48V
Classification: IACT
OSMANTHUS FRAGRANS FLOWERInactive
Code: 4VA0BH57HU
Classification: IACT
EUCALYPTUS OILInactive
Code: 2R04ONI662
Classification: IACT
BORNEOLActive
Quantity: 1.2 g in 100 1
Code: M89NIB437X
Classification: ACTIB