NDC Code(s) : 66949-207-24
Packager : Zep Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Zep Professional Z-Verdant FoamingTriclosan LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66949-207
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN(UNII: 4NM5039Y5X)
(TRICLOSAN - UNII:4NM5039Y5X) 		TRICLOSAN0.01 g in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
TRIETHANOLAMINE LAURYL SULFATE(UNII: E8458C1KAA)
PEG-7 GLYCERYL COCOATE(UNII: VNX7251543)
TETRASODIUM IMINODISUCCINATE(UNII: GYS41J2635)
METHYLCHLOROISOTHIAZOLINONE(UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE(UNII: 229D0E1QFA)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
GLUTARAL(UNII: T3C89M417N)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:66949-207-243785 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product06/08/2009
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 06/08/2009 01/01/2019

PRINCIPAL DISPLAY PANEL

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