Label: KUTKIT- aluminum sulfate swab

  • NDC Code(s): 10705-301-50
  • Packager: Majestic Drug Co., Inc.
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 24, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Aluminum Sulfate 51%

  • Purpose

    Astringent

  • Use

    Stops bleeding caused by minor surface cuts and abrasions as may occur during shaving.

  • Warnings

    For external use only.

    When using this product

    • Avoid contact with eyes. If contact occurs rinse thoroughly with water.
    • Stings when applied. For minor cuts and scrapes only.

    Stop use and ask a doctor if bleeding persists or redness, irritation or swelling occurs.

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

  • Directions

    For best results

    • Slightly moisten the swab with water.
    • Count to 3.
    • Apply directly to the affected area.

    Note: Swab may be used dry if necessary.

  • Inactive Ingredient

    Water.

  • PRINCIPAL DISPLAY PANEL - 24 Swab Box

    SANITARY
    KUTKIT®
    Astringent

    STYPTIC SWABS

    STOPS
    BLEEDING
    INSTANTLY

    • SHAVING NICKS
    • CUTICLES
    • MINOR CUTS

    24 SWABS

    Principal Display Panel - 24 Swab Box
  • INGREDIENTS AND APPEARANCE
    KUTKIT 
    aluminum sulfate swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10705-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Aluminum Sulfate (UNII: 34S289N54E) (ALUMINUM SULFATE ANHYDROUS - UNII:I7T908772F) Aluminum Sulfate0.047 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10705-301-5024 in 1 BOX; Type 0: Not a Combination Product11/07/202012/31/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34711/07/202012/31/2023
    Labeler - Majestic Drug Co., Inc. (001496777)