Label: AVANCE CURE INCONTINENCE- allantoin, dimethicone cream
- NDC Code(s): 70936-105-11, 70936-105-12, 70936-105-22
- Packager: SMART CHOICE MEDICAL INC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 7, 2024
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- ACTIVE INGREDIENT:
- PURPOSE:
- USES
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
-
INACTIVE INGREDIENTS:
ALOE BARBADENSIS (ALOE VERA) LEAF JUICE, BUTYROSPERMUN PARKII (SHEA BUTTER), GLYCERIN,
BEESWAX, CETEARYL ALCOHOL, CARTHAMUS TINDORIUS (SAFFLOWER) SEED OIL, POLYSORBATE 60,
MAGNESIUM ALUMINUM SILICATE, ZINC PCA, AVENA SATIVA (OAT) KERNEL FLOUR, SODIUM PCA,
PANTHENOL (VITAMIN B5), TOCOPHERYL ACETATE (VITAMIN E), SODIUM HYALURONATE, GLYCERYL STEARATE,
SOBIC ACID, SODIUM PHYTATE, XANTHAN GUM, PHENOXYETHANOL, ETHYHEXYLGLYCERIN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVANCE CURE INCONTINENCE
allantoin, dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70936-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 1.5 g in 100 g DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 2 g in 100 g Inactive Ingredients Ingredient Name Strength PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) SORBIC ACID (UNII: X045WJ989B) PHYTATE SODIUM (UNII: 88496G1ERL) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE VERA LEAF (UNII: ZY81Z83H0X) SHEA BUTTER (UNII: K49155WL9Y) GLYCERIN (UNII: PDC6A3C0OX) WHITE WAX (UNII: 7G1J5DA97F) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) POLYSORBATE 60 (UNII: CAL22UVI4M) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) ZINC PIDOLATE (UNII: C32PQ86DH4) OATMEAL (UNII: 8PI54V663Y) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70936-105-11 135 g in 1 TUBE; Type 0: Not a Combination Product 08/23/2016 2 NDC:70936-105-12 270 g in 1 TUBE; Type 0: Not a Combination Product 08/23/2016 3 NDC:70936-105-22 270 g in 1 JAR; Type 0: Not a Combination Product 08/23/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 08/23/2016 Labeler - SMART CHOICE MEDICAL INC. (046383276) Registrant - SMART CHOICE MEDICAL INC. (046383276)