Vexa
Vexa-D
Approved
Approval ID
85933294-59de-4465-a02c-4225f0c20ce8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 24, 2015
Manufacturers
FDA
Pharmaceutics Corporation
DUNS: 079132026
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Lidocaine, Allantoin, Petrolatum
PRODUCT DETAILS
NDC Product Code49430-053
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateMarch 20, 2015
Generic NameLidocaine, Allantoin, Petrolatum
INGREDIENTS (5)
ALLANTOINActive
Quantity: 2 mg in 1 1
Code: 344S277G0Z
Classification: ACTIB
LIDOCAINEActive
Quantity: 4 mg in 1 1
Code: 98PI200987
Classification: ACTIB
PETROLATUMActive
Quantity: 30 mg in 1 1
Code: 4T6H12BN9U
Classification: ACTIB
ONIONInactive
Code: 492225Q21H
Classification: IACT
.ALPHA.-TOCOPHEROLInactive
Code: H4N855PNZ1
Classification: IACT