Label: DIABETIC FOOT CREAM- dimethicone cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 19, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Dimethicone 1%..............................Skin Protectant

  • Purpose

    Skin Protectant

  • Uses

    Helps prevent and temporarily protects chafed, chapped, or cracked skin.

  • Warnings

    For external use only.

  • When using this product

    do not get into the eyes

  • Stop use and ask physician if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
  • Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns
  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply as needed.

  • Other information

    Store at 20° – 25°C (68° – 77°F).

  • Inactive Ingredients

    Water, Propanediol, Ricinus Communis (Castor) Seed Oil, Lauryl Laurate, Arachidyl Alcohol, Inula Viscosa Flower/Leaf/Stem Extract, Stearyl Alcohol, Behenyl Alcohol, Glycerin, Synthetic Beeswax, Arachidyl Glucoside, Cetyl Alcohol, Copernicia Cerifera (Carnauba) Wax, Euphorbia Cerifera (Candelilla) Wax, Limonene, Sodium Benzoate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Potassium Sorbate, Disodium EDTA, Xanthan Gum, Hydrolyzed Vegetable Protein, Citrus Aurantium Dulcis (Orange) Peel Oil, Leuconostoc/Radish Root Ferment Filtrate, Linalool, Citral

  • Questions?

    Call toll free 1-844-474-2552 or visit www.lavior.com

  • PRINCIPAL DISPLAY PANEL

    Diabetic Foot Cream

  • INGREDIENTS AND APPEARANCE
    DIABETIC FOOT CREAM 
    dimethicone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71521-392
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LAURYL LAURATE (UNII: GPW77G0937)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    CITRAL (UNII: T7EU0O9VPP)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71521-392-10100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/31/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/31/2021
    Labeler - Lavior Pharma Inc (080685327)