Label: AVANCE CURE MOISTURIZING INCONTINENCE CREAM- allantoin, dimethicone cream
- NDC Code(s): 70936-108-11, 70936-108-12, 70936-108-22
- Packager: SMART CHOICE MEDICAL INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
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- ACTIVE INGREDIENT:
- PURPOSE:
- USES
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS:
Prepare the affected area by gently cleaning the skin surface before use. Apply a proper amount of cream to affected area. Spread the cream across the affected area by gently rubbing on the irritated skin. Repeat the process as needed, or daily to ensure constant protection until the skin is healed.
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INACTIVE INGREDIENTS:
Water, Butyrospermum Parkii Extract (Shea Butter), Aloe barbadensis (Aloe Vera), Maltodextrin, Glycerin, Glyceryl stearate, Bee Wax, Safflower oil, Pyrrolidone Carboxylic Acid-Na, Cetearyl alcohol, Sodium Polyglutamate, 1,3- Butylene Glycol, Panthenol, Tocopheryl Acetate, Xanthan gum, Ethylhexylglycerin, Phenoxyethanol, Ceteareth - 20, Sodium hyaluronate, Glyceryl glucoside, Avena Sativa (Oat) Protein Extract, Lactobacillus/Soymilk Ferment Filtrate, Bacillus/Soybean Ferment Extract, Propanediol, 1,2-Hexanediol
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INGREDIENTS AND APPEARANCE
AVANCE CURE MOISTURIZING INCONTINENCE CREAM
allantoin, dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70936-108 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 MALTODEXTRIN (UNII: 7CVR7L4A2D) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) YELLOW WAX (UNII: 2ZA36H0S2V) SAFFLOWER OIL (UNII: 65UEH262IS) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) HYALURONATE SODIUM (UNII: YSE9PPT4TH) .BETA.-D-GLUCOPYRANOSE (UNII: J4R00M814D) OAT (UNII: Z6J799EAJK) SOYBEAN (UNII: L7HT8F1ZOD) PROPANEDIOL (UNII: 5965N8W85T) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) WATER (UNII: 059QF0KO0R) SHEA BUTTER (UNII: K49155WL9Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70936-108-11 135 g in 1 TUBE; Type 0: Not a Combination Product 07/02/2018 2 NDC:70936-108-12 270 g in 1 TUBE; Type 0: Not a Combination Product 07/02/2018 3 NDC:70936-108-22 270 g in 1 JAR; 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 Drug M016 08/22/2016 Labeler - SMART CHOICE MEDICAL INC. (046383276) Registrant - SMART CHOICE MEDICAL INC. (046383276)