AVANCE INCONTINENCE CARE- benzethonium chloride cream

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 0.20% (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

• APPPLY CREAM TO AFFECTED AREA. RUB IN GENTLY.

OTHER INFORMATION

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

INACTIVE INGREDIENTS

Water, Helianthus Annuus Seed Oil, Cetearyl Alcohol, Stearic Acid, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Butylene Glycol, Urea, Zinc PCA, Aloe Barbadensis Leaf Juice, Allantoin, Panthenol, Arginine, Niacinamide, Butyrospermum
Parkii (Shea) Butter, Tocopheryl Acetate, Polysorbate 60, Salvia Officinalis (Sage) Leaf Extract, Equisetum Arvense Extract, Citrus Limon (Lemon) Fruit Extract, Acacia Senegal Gum, Xanthan Gum, Citric Acid, Ethylhexylglycerin, Phenoxyethanol, Potassium Sorbate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVANCE INCONTINENCE CARE 
benzethonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70936-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PANTHENOL (UNII: WV9CM0O67Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SHEA BUTTER (UNII: K49155WL9Y)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-100 STEARATE (UNII: YD01N1999R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
UREA (UNII: 8W8T17847W)
POLYSORBATE 60 (UNII: CAL22UVI4M)
ZINC PIDOLATE (UNII: C32PQ86DH4)
ALLANTOIN (UNII: 344S277G0Z)
ARGININE (UNII: 94ZLA3W45F)
SUNFLOWER OIL (UNII: 3W1JG795YI)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
NIACINAMIDE (UNII: 25X51I8RD4)
SAGE (UNII: 065C5D077J)
LEMON JUICE (UNII: AGN709ANTJ)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ACACIA (UNII: 5C5403N26O)
EQUISETUM ARVENSE WHOLE (UNII: 73DM367W4P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70936-111-95	270 g in 1 JAR; Type 0: Not a Combination Product	06/29/2022
2	NDC: 70936-111-27	270 g in 1 TUBE; 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)