NDC Code(s) : 66949-999-00, 66949-999-10, 66949-999-21, 66949-999-15, 66949-999-89
Packager : Zep Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Zep AcclaimTriclosan LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66949-999
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)
AMMONIUM CHLORIDE(UNII: 01Q9PC255D)
DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE(UNII: 1YHW4GJC3U)
GLYCERIN(UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID(UNII: XF417D3PSL)
METHYLCHLOROISOTHIAZOLINONE(UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE(UNII: 229D0E1QFA)
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:66949-999-00500 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product29/03/1995
2NDC:66949-999-101000 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product29/03/1995
3NDC:66949-999-213785 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product29/03/1995
4NDC:66949-999-15946.353 mL in 1 BOTTLE Type 0: Not a Combination Product29/03/1995
5NDC:66949-999-891040990 mL in 1 CONTAINER Type 0: Not a Combination Product29/03/1995
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 03/29/1995 01/01/2019

PRINCIPAL DISPLAY PANEL

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