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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49430-053
Product Classification
G
Generic Name
Lidocaine, Allantoin, Petrolatum
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 20, 2015
FDA Product Classification
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