VANOXIDE
SUMMERS LABS (as PLD) - VANOXIDE (11086-032)
Approved
Approval ID
1f0edbd9-103e-4a49-b7a8-6552ef172c13
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 9, 2023
Manufacturers
FDA
Summers Laboratories Inc
DUNS: 002382612
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
BENZOYL PEROXIDE, HYDROCORTISONE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code11086-032
Product Classification
G
Generic Name
BENZOYL PEROXIDE, HYDROCORTISONE
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 9, 2023
FDA Product Classification
INGREDIENTS (2)
BENZOYL PEROXIDEActive
Quantity: 5 g in 100 g
Code: W9WZN9A0GM
Classification: ACTIB
HYDROCORTISONEActive
Quantity: 0.5 g in 100 g
Code: WI4X0X7BPJ
Classification: ACTIB