AVANCE INCONTINENCE CARE- benzethonium chloride solution

AVANCE INCONTINENCE CARE by

Drug Labeling and Warnings

AVANCE INCONTINENCE CARE 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% (W/W)

PURPOSE

ANTISEPTIC

USES

• PREVENTS SKIN INFECTION
• KILLS GERMS

WARNINGS

• FOR EXTERNAL ONLY

DO NOT USE:

• ON WILD OR DOMESTIC ANIMAL BITES. IF YOU HAVE AN ANIMAL BITE, CONSULT YOUR PHYSICIAN IMMEDIATELY.
• ON INFECTIONS
• FOR MORE THAN 10 DAYS. IF INFECTION WORSENS OR PERSISTS, SEE YOUR PHYSICIAN.

WHEN USING THIS PRODUCT:

• AVOID CONTACT WITH EYES

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

• Apply to affected area
• Spray on a clean cloth and remove urine, feces and vomit.
• Cleanse skin of all residue and wipe with clean cloth to dry. If the surface area is massive, rinse affected area with warm water before using.

OTHER INFORMATION

• STORE AT ROOM TEMPERATURE
• USE ON INFANTS, CHILDREN OR ADULTS

INACTIVE INGREDIENTS

Water, Polysorbate 60, Sodium Methyl Cocoyl Taurate, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Juice, Zinc PCA, Allantoin, Panthenol, Glycerin, Butylene Glycol, PEG-12 Dimethicone, Citric Acid, Ethylhexylglycerin, Fragrance, Phenoxyethanol, Potassium Sorbate.

QUESTIONS?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVANCE INCONTINENCE CARE 
benzethonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70936-112
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 g

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PANTHENOL (UNII: WV9CM0O67Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POLYSORBATE 60 (UNII: CAL22UVI4M)
ZINC PIDOLATE (UNII: C32PQ86DH4)
ALLANTOIN (UNII: 344S277G0Z)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70936-112-08	237 g in 1 BOTTLE; Type 0: Not a Combination Product	06/29/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/29/2022

Labeler - SMART CHOICE MEDICAL INC. (046383276)