NeoBenz(R) Micro
Approved
Approval ID
375bf717-5d70-457e-8b74-1f66f4f08b79
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 6, 2009
Manufacturers
FDA
SkinMedica Pharmaceuticals, Inc., Carlsbad, CA 92010
DUNS: 124977005
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
benzoyl peroxide, 7%
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67402-027
Product Classification
G
Generic Name
benzoyl peroxide, 7%
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 6, 2009
FDA Product Classification
INGREDIENTS (1)
BENZOYL PEROXIDEActive
Quantity: 70 mg in 1 g
Code: W9WZN9A0GM
Classification: ACTIB