DERMAWERX ZMT PAK
Approved
Approval ID
24682288-1be4-42af-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 13, 2015
Manufacturers
FDA
Patchwerx Labs, Inc.
DUNS: 079584480
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ZINC OXIDE, MENTHOL, UNSPECIFIED FORM, and TRETINOIN
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69329-600
Application NumberANDA075264
Product Classification
M
Marketing Category
C73584
G
Generic Name
ZINC OXIDE, MENTHOL, UNSPECIFIED FORM, and TRETINOIN
Product Specifications
Effective DateNovember 13, 2015
FDA Product Classification