NDC Code(s) : 66949-277-01
Packager : Zep Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Zep Mango FoamingTriclosan LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66949-277
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)
AMMONIUM LAURYL SULFATE(UNII: Q7AO2R1M0B)
AMMONIUM LAURETH-3 SULFATE(UNII: 896SJ235FN)
COCO DIISOPROPANOLAMIDE(UNII: S485AM948Q)
DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE(UNII: 1YHW4GJC3U)
GLYCERIN(UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE(UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE(UNII: DEL7T5QRPN)
ANHYDROUS CITRIC ACID(UNII: XF417D3PSL)
GLUTARAL(UNII: T3C89M417N)
FD&C YELLOW NO. 5(UNII: I753WB2F1M)
FD&C RED NO. 4(UNII: X3W0AM1JLX)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:66949-277-01550 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product02/01/2010
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 02/01/2010 01/02/2019

PRINCIPAL DISPLAY PANEL

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