4% lidocaine plus 1% menthol Pain Relief Patch
Approved
Approval ID
2f98ee5e-e4eb-fbda-e063-6394a90a709c
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Mar 5, 2025
Manufacturers
FDA
Xuzhou Lanting Pharmaceutical Co., Ltd
DUNS: 457641059
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Pain Relief Patch, Pain Relief Strip
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code85323-003
Application NumberM017
Product Classification
M
Marketing Category
C200263
G
Generic Name
Pain Relief Patch, Pain Relief Strip
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 5, 2025
FDA Product Classification
INGREDIENTS (15)
SODIUM POLYACRYLATE (2500000 MW)Inactive
Code: 05I15JNI2J
Classification: IACT
TARTARIC ACIDInactive
Code: W4888I119H
Classification: IACT
LEVOMENTHOLActive
Quantity: 1 g in 100 g
Code: BZ1R15MTK7
Classification: ACTIB
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUSInactive
Code: 1K713C615K
Classification: IACT
KAOLINInactive
Code: 24H4NWX5CO
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
EDETATE DISODIUMInactive
Code: 7FLD91C86K
Classification: IACT
CARBOMERInactive
Code: 0A5MM307FC
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
POVIDONE K90Inactive
Code: RDH86HJV5Z
Classification: IACT
LIDOCAINE HYDROCHLORIDEActive
Quantity: 4 g in 100 g
Code: V13007Z41A
Classification: ACTIR
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
CARBOXYMETHYLCELLULOSE SODIUMInactive
Code: K679OBS311
Classification: IACT
DMDM HYDANTOINInactive
Code: BYR0546TOW
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT