Lynx Antibacterial
Lynx Antibacterial Hand Soap 6544 Drug Facts and Label
Approved
Approval ID
b469cfb7-35bf-419d-b1dc-95dcfad611f5
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 22, 2025
Manufacturers
FDA
ABC Compounding Co., Inc.
DUNS: 003284353
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
CHLOROXYLENOL
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62257-160
Application NumberM003
Product Classification
M
Marketing Category
C200263
G
Generic Name
CHLOROXYLENOL
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 22, 2025
FDA Product Classification
INGREDIENTS (10)
SODIUM LAURETH SULFATEInactive
Code: BPV390UAP0
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
COCO MONOISOPROPANOLAMIDEInactive
Code: 21X4Y0VTB1
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
DMDM HYDANTOINInactive
Code: BYR0546TOW
Classification: IACT
DECYL GLUCOSIDEInactive
Code: Z17H97EA6Y
Classification: IACT
CITRIC ACID MONOHYDRATEInactive
Code: 2968PHW8QP
Classification: IACT
FD&C YELLOW NO. 5Inactive
Code: I753WB2F1M
Classification: IACT
CHLOROXYLENOLActive
Quantity: 3 mg in 1 mL
Code: 0F32U78V2Q
Classification: ACTIB