NDC Code(s) : 54565-2201-2, 54565-2201-7, 54565-2201-1
Packager : Les Emballages Knowlton Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Ban Aluminum Chlorohydrate LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:54565-2201
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE(UNII: HPN8MZW13M)
(ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) 		ALUMINUM CHLOROHYDRATE20 g in 103 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
STEARETH-2(UNII: V56DFE46J5)
STEARETH-20(UNII: L0Q8IK9E08)
SANDALWOOD(UNII: 3641YW25N2)
PHELLODENDRON AMURENSE BARK(UNII: PBG27B754G)
BARLEY(UNII: 5PWM7YLI7R)
PPG-11 STEARYL ETHER(UNII: S4G2J0Y0LG)
SUNFLOWER OIL(UNII: 3W1JG795YI)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:54565-2201-2103 mL in 1 BOTTLE, WITH APPLICATOR Type 0: Not a Combination Product01/01/2012
2NDC:54565-2201-72 in 1 PACKAGE 09/12/2016
2103 mL in 1 BOTTLE, WITH APPLICATOR Type 0: Not a Combination Product01/01/2012
3NDC:54565-2201-144 mL in 1 BOTTLE, WITH APPLICATOR Type 0: Not a Combination Product11/04/2016
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 01/01/2012

PRINCIPAL DISPLAY PANEL

ban

unscented

ROLL-ON

ANTIPERSPIRANT

DEODORANT

3.5 FL OZ (103 mL)

10596-338-UPDATED