AVANCE CURE FOAMING BODY CLEANSER- benzethonium chloride solution

Avance Cure Foaming Body Cleanser by

Drug Labeling and Warnings

Avance Cure Foaming Body Cleanser 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:

Benzethonium chloride 0.12%

PURPOSE:

ANTIBACTERIAL

USES

Assists in the odor and skin treatment of incontinent and bedridden patients.
Provides moisture to prevent skin breakdown, usually caused by sweat and urine acidity.
Protects the skin from breakdown and dryness.

WARNINGS:

For external use only

Do not use:
On Deep Open Wounds
On Infections
On Skin Lacerations

When using this product:
Avoid contact with eyes

Stop use and ask a doctor if:
Condition worsens or does not improve within 7 days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:
If swallowed or ingested, seek medical attention or contact the Poison Control Center immediately.

DIRECTIONS:

Prepare the affected area by gently cleaning the skin surface before use. Apply a proper amount of foam to the cleansing area. Spread across the area by gently applying on the irritated skin. Repeat the process as needed, or daily to ensure constant protection until the skin is healed.

QUESTIONS?

Call 1-800-768-3801 or visit smartchoicemedical.com

INACTIVE INGREDIENTS:

Water, Propylene Glycol, Citric Acid, Fragrance, Aloe barbadensis Leaf Juice, Maltodextrin, Sodium Polyglutamate, 1,3 Butylene glycol, Ethylhexylglycerin, Phenoxyethanol, Decyl Glucoside, DMDM Hydantoin, Disodium Cocoamphodiacetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVANCE CURE FOAMING BODY CLEANSER 
benzethonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70936-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MONOSODIUM DL-GLUTAMATE (UNII: LX3YQ006AP)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70936-110-11	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/02/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/22/2016

Labeler - SMART CHOICE MEDICAL INC. (046383276)

Registrant - SMART CHOICE MEDICAL INC. (046383276)