Renuu NL
RENUU NL
Approved
Approval ID
172e582c-7e76-38ac-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 28, 2015
Manufacturers
FDA
Patchwerx Labs
DUNS: 079584480
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ALLANTOIN, PETROLATUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69329-011
Product Classification
G
Generic Name
ALLANTOIN, PETROLATUM
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 28, 2015
FDA Product Classification
INGREDIENTS (4)
.ALPHA.-TOCOPHEROLInactive
Code: H4N855PNZ1
Classification: IACT
ONIONInactive
Code: 492225Q21H
Classification: IACT
PETROLATUMActive
Quantity: 30 g in 100 g
Code: 4T6H12BN9U
Classification: ACTIB
ALLANTOINActive
Quantity: 2 g in 100 g
Code: 344S277G0Z
Classification: ACTIB