Label: DERMELEVE- aluminum acetate cream

  • NDC Code(s): 81507-003-01, 81507-003-02
  • Packager: Advanced Derm Solutions LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 29, 2025

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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 

    Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Caprylyl Glycol, Ceramide NG, Cetearyl Alcohol, Cetyl Alcohol, Citric Acid

    Dimethicone, Disodium EDTA, Glycerin, Glyceryl Stearate, Isopropyl Myristate, Magnesium Aluminum Silicate, Phenoxyethanol, Polyacrylate

    Crosspolymer-6, Polysorbate 60, Sodium Hyaluronate, Strontium Nitrate, Tetrahexyldecyl Ascorbate, Titanium Dioxide, Tocopheryl Acetate

    Water, 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 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
    SHEA BUTTER (UNII: K49155WL9Y)  
    TRICAPRIN (UNII: O1PB8EU98M)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CERAMIDE NG (UNII: C04977SRJ5)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    STRONTIUM NITRATE (UNII: BDG873AQZL)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81507-003-01120 g in 1 TUBE; Type 0: Not a Combination Product02/04/2022
    2NDC:81507-003-02113 g in 1 TUBE; Type 0: Not a Combination Product05/28/2025
    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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