Label: EXEMAX CREAM- dimethicone, allantoin cream

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

Drug Label Information

Updated July 1, 2025

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  • DESCRIPTION

    Drug Facts

  • Active Ingredients

    Dimethicone 5%
    Allantoin 2%

  • Purpose

    Skin Protectant

  • Uses

    ● temporarily protects and helps relieve chapped or cracked skin
    ● helps protect from the drying effects of wind and cold weather

  • Warnings

    ● For external use only

    When using this product

    ● do not get into eyes.

    Stop use and ask a doctor 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 20º-25ºC (68º-77ºF) [see USP Controlled Room Temperature]

  • Inactive ingredients:

    Aqua (Purified Water), Arnica Montana (Arnica) Flower Extract, Avena sativa (Oat) Kernel Flour, Bisabolol, Calcium Pantothenate (Vitamin B5), Carthamus tinctorius (Safflower) Oleosomes, Centella Asiatica (Asiatic Pennywort) Extract, Citric Acid, DL-Alpha-Tocopheryl Acetate (Vitamin E), Ethylhexylglycerin, Glycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Inositol, Lactic Acid, Maltodextrin, Niacinamide (Vitamin B3), Phenoxyethanol, Polyacrylate Crosspolymer-6, Pyridoxine HCl (Vitamin B6), Saccharide Isomerate, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Ascorbyl Phosphate (Vitamin C), Sodium Citrate, Sodium Hyaluronate, Sodium Hydroxide, Sodium Starch Octenylsuccinate, Tetrahexyldecyl Ascorbate, Zingiber Officinale (Ginger) Root Extract.

  • Exemax™ Cream

    Manufactured by:
    PureTek Corporation
    Panorama City, CA 91402
    For questions or information
    call toll-free: 877-921-7873

    Label

  • INGREDIENTS AND APPEARANCE
    EXEMAX CREAM 
    dimethicone, allantoin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-212
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN2 g  in 100 g
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    GINGER (UNII: C5529G5JPQ)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    OAT (UNII: Z6J799EAJK)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PYRIDOXINE HCL (UNII: 68Y4CF58BV)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    BISABOLOL (UNII: 24WE03BX2T)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    INOSITOL (UNII: 4L6452S749)  
    SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59088-212-0785 g in 1 TUBE; Type 0: Not a Combination Product07/02/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01607/02/2025
    Labeler - PureTek Corporation (785961046)
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