Label: DERMELEVE- aluminum acetate cream

  • NDC Code(s): 81507-003-01
  • Packager: Advanced Derm Solutions LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2023

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  • Active Ingredient

    Aluminum acetate (0.2%)

  • Purpose

    Astringent

  • Uses

    • Insects Bites
    • Minor Burn
    • Athlete's foot 
    • Poison lvy 
    • Poison oak
    • Poison sumac 
    • Rashes cause by soaps, detergents, cosmetic or jewelry

  • Warnings

    ■ For external use only.
    ■ Avoidcontact with eyes.
    ■ Do not applyto open wounds.
    ■ STOP USEand ask a physician if condition worsens
    or symptoms persist for more than seven days.

    ■ Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Adults and children two years of age and older,
    apply to affected area as needed or as directed by a physician. Consult a physician for children under the age of two.

  • Inactive ingredients 

    Caprylyc/Capric Triglyceride, Caprylyl Glycol, Ceramide NG, Cetearyl Alcohol, Dimethicone 100,
    Disodium Edta, Emulsifying Wax NF, Glycerin, Glyceryl Stearate SE, Sodium Hyaluronate, Isopropyl Myristate Magnesium Aluminum Silicate Type IA, Phenoxyethanol, Polyacrylate Crosspolymer-6, Shea Butter, Strontium Nitrate, Tetrahexyldecyl Ascorbate, Tocopherol, Water O-18, Xanthan Gum

  • SPL UNCLASSIFIED SECTION

    Questions ?  Visit  www.dermeleve.com

  • SPL UNCLASSIFIED SECTION

    Manufactured for Advanced Derm Solutions LLC
    Oldsmar, FL 34677 | dermeleve.com
    U.S. Patents: 5,716,625; 5,804,203; 6,139,850; 7,404,967

  • Product label

    image descriptionimage descriptionimage descriptionimage descriptionimage description

  • INGREDIENTS AND APPEARANCE
    DERMELEVE 
    aluminum acetate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81507-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE0.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CERAMIDE NG (UNII: C04977SRJ5)  
    DIMETHICONE 100 (UNII: RO266O364U)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    MAGNESIUM ALUMINUM SILICATE TYPE IA (UNII: SUS08ZOA9S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    STRONTIUM NITRATE (UNII: BDG873AQZL)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER O-18 (UNII: 7QV8F8BYNJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLAWAX POLYSORBATE (UNII: Q504PL8E0V)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81507-003-01120 g in 1 TUBE; Type 0: Not a Combination Product02/04/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01602/04/2022
    Labeler - Advanced Derm Solutions LLC (117840544)
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