Label: DOMEBORO- aluminum sulfate tetradecahydrate, calcium acetate monohydrate powder, for solution

  • NDC Code(s): 16864-240-01, 16864-240-10, 16864-240-14
  • Packager: Advantice Health, LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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

  • SPL UNCLASSIFIED SECTION

  • ACTIVE INGREDIENT

    Active Ingredients (in each packet)Purpose
    Aluminum sulfate tetradecahydrate, 1347 mgAstringent*
    Calcium acetate monohydrate, 952 mgAstringent*
    *When combined together in water, these ingredients form the active ingredient aluminum acetate. See Directions.
  • Uses

    temporarily relieves minor skin irritations due to:

    • poison ivy
    • poison oak
    • poison sumac
    • insect bites
    • athlete's foot
    • rashes caused by soaps, detergents, cosmetics, or jewelry
  • Warnings

    For external use only

    Whenusing this product

    • avoid contact with eyes. If contact occurs, rinse thoroughly with water.
    • do not cover compress or wet dressing with plastic to prevent evaporation
    • in some skin conditions, soaking too long may overdry

    Stop use and ask a doctor ifcondition worsens or symptoms persist for more than 7 days

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • dissolve 1 to 3 packets in a pint (16 oz) of cool or warm water
    • stir until fully dissolved; do not strain or filter. The resulting mixture contains 0.16% (1 packet), 0.32% (2 packets), or 0.48% (3 packets) aluminum acetate and is ready for use.              

    For use as a soak:

    • soak affected area for 15 to 30 minutes as needed, or as directed by a doctor
    • repeat 3 times a day or as directed by a doctor
    • discard solution after each use

    For use as a compress or wet dressing:

    • soak a clean, soft cloth in the solution
    • apply cloth loosely to affected area for 15 to 30 minutes
    • repeat as needed or as directed by a doctor
    • discard solution after each use
  • STORAGE AND HANDLING

    Other informationprotect from excessive heat

  • INACTIVE INGREDIENT

    Inactive ingredientsdextrin

  • Questions or comments?

    1-800-345-0032
    www.domeboro.com

  • SPL UNCLASSIFIED SECTION

    Distributed by Advantice Health, LLC Cedar Knolls, NJ 07927

  • PRINCIPAL DISPLAY PANEL - 12 Packet Box

    DOCTOR RECOMMENDED
    DOMEBORO ®
    Aluminum Sulfate Tetradecahydrate / Calcium Acetate Monohydrate-Astringent

    Burow's Solution
    Relief Since 1958

    CALMING & SOOTHING
    Medicated Soak

    RASH RELIEF
    PLUS DRYING ACTION

    EFFECTIVE FOR POISON IVY, OAK,
    SUMAC & OTHER RASHES

    Dries Oozing
    Rashes

    Relieves Itching
    & Burning

    Reduces
    Blistering

    12 POWDER
    PACKETS

    RELIEF AT LAST

    NET WT 0.1 OZ
    (2.7 G) EACH

    PRINCIPAL DISPLAY PANEL - 12 Packet Box
  • INGREDIENTS AND APPEARANCE
    DOMEBORO 
    aluminum sulfate tetradecahydrate, calcium acetate monohydrate powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16864-240
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SULFATE TETRADECAHYDRATE (UNII: E3UT66504P) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM SULFATE TETRADECAHYDRATE1347 mg
    CALCIUM ACETATE MONOHYDRATE (UNII: 7ZA48GIM5H) (ACETATE ION - UNII:569DQM74SC) CALCIUM ACETATE MONOHYDRATE952 mg
    Inactive Ingredients
    Ingredient NameStrength
    ICODEXTRIN (UNII: 2NX48Z0A9G)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:16864-240-0112 in 1 BOX; Type 0: Not a Combination Product06/26/2012
    2NDC:16864-240-10100 in 1 BOX; Type 0: Not a Combination Product06/26/201204/30/2017
    3NDC:16864-240-1414 in 1 BOX; Type 0: Not a Combination Product06/26/201207/31/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01606/26/2012
    Labeler - Advantice Health, LLC. (192527062)