AVANCE CURE ANTI-BACTERIAL PERINEAL- benzalkonium chloride spray

AVANCE CURE ANTI-BACTERIAL PERINEAL by

Drug Labeling and Warnings

AVANCE CURE ANTI-BACTERIAL PERINEAL by is a Otc medication manufactured, distributed, or labeled by SMART CHOICE MEDICAL INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

• BENZALKONIUM CHLORIDE              0.3%

PURPOSE:

ANTIBACTERIAL

USES

INCONTINENT/OSTOMY CLEANSER, FORMULATED TO COOL AND SOOTHE SKIN, AVENCE CURE ANTI-BACTERIAL PERINEAL SPRAY REDUCES THE RISK OF SKIN IRRITATIONS AND RASHES. AVANCE CURE ANTI-BACTERIAL PERINEAL SPRAY GENTLY HELPS CLEANSE SKIN OF BODILY WASTES, AND PROTECTS AGAINST HARMFUL BACTERIA.

WARNINGS:

• FOR EXTERNAL ONLY

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDERN:

• IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY

DIRECTIONS:

PERINEAL AREA: SPRAY ONTO THE AREA TO BE CLEANED. GENTLY REMOVE ANY RESIDUE AND WIPE CLEAN WITH MOIST CLOTH. REPEAT AS NEEDED.

INACTIVE INGREDIENTS:

DISODIUM LAURETH SULFOSUCCINATE

COCAMIDOPROPYL BETAINE

GLYCERIN

ALOE BARBADENSIS (ALOE) LEAF JUICE

PHENOXYETHANOL

ETHYLHEXYLGLYCERIN

FRAGRANCE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVANCE CURE ANTI-BACTERIAL PERINEAL 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70936-107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70936-107-11	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/22/2016
2	NDC: 70936-107-12	240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/22/2016
3	NDC: 70936-107-13	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/22/2016
4	NDC: 70936-107-14	960 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/22/2016

Labeler - SMART CHOICE MEDICAL INC. (046383276)

Registrant - SMART CHOICE MEDICAL INC. (046383276)