NDC Code(s) : 10056-178-10
Packager : Access Business Group, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Body Series Deodorant and Antiperspirant Roll-On ALUMINUM CHLOROHYDRATE LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10056-178
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE(UNII: HPN8MZW13M)
(ALUMINUM CATION - UNII:3XHB1D032B) 		ALUMINUM CHLOROHYDRATE25 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
PROPYLENE GLYCOL DIETHYLHEXANOATE(UNII: 8D8I9Z0F1Z)
STEARETH-2(UNII: V56DFE46J5)
STEARETH-20(UNII: L0Q8IK9E08)
ALCLOXA(UNII: 18B8O9DQA2)
GLYCINE(UNII: TE7660XO1C)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
USNEA BARBATA(UNII: D6DVA9TCAP)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:10056-178-10100 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 04/11/2011

PRINCIPAL DISPLAY PANEL

Body Series

Deodorant and AnitPerspirant

Roll-On

Regular Scent

Made In U.S.A.

100mL (3.38 fl oz)

PRINCIPAL DISPLAY PANEL

Body Series Roll On

PRINCIPAL DISPLAY PANEL

Body Series Roll-On