NDC Code(s) : 43333-462-16
Packager : Tonic Bath and Body Products Shenzhen Ltd.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Antibacterial Foaming Hand Wash CranberryBenzalkonium Chloride LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43333-462
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE(UNII: F5UM2KM3W7)
(BENZALKONIUM - UNII:7N6JUD5X6Y) 		BENZALKONIUM CHLORIDE1 mg in 13 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF(UNII: ZY81Z83H0X)
OXYBENZONE(UNII: 95OOS7VE0Y)
CITRIC ACID ACETATE(UNII: DSO12WL7AU)
COCAMIDOPROPYL BETAINE(UNII: 5OCF3O11KX)
COCAMIDOPROPYLAMINE OXIDE(UNII: M4SL82J7HK)
WATER(UNII: 059QF0KO0R)
EDETIC ACID(UNII: 9G34HU7RV0)
D&C RED NO. 33(UNII: 9DBA0SBB0L)
GLYCERIN(UNII: PDC6A3C0OX)
WITCH HAZEL(UNII: 101I4J0U34)
METHYLCHLOROISOTHIAZOLINONE(UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE(UNII: 229D0E1QFA)
OLEA EUROPAEA LEAF(UNII: MJ95C3OH47)
PANTHENOL(UNII: WV9CM0O67Z)
POLYSORBATE 20(UNII: 7T1F30V5YH)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SODIUM LAURAMINOPROPIONATE(UNII: X5NJA9HXPU)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:43333-462-16500 mL in 1 BOTTLE, PUMP Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 08/24/2015

PRINCIPAL DISPLAY PANEL

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