Label: ALCOHOL PREP PAD- isopropyl alcohol swab

  • 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 16, 2013

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Isopropyl alcohol 70%

  • Purpose

    First aid antiseptic

  • Uses

    first aid to help prevent infection in minor

    • cuts
    • scrapes
    • burns
  • Warnings

    For external use only.

    Caution

    FLAMMABLE. Keep away from fire or flame.

    Do not use

    • in the eyes
    • longer than 1 week
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wound
    • animal bite
    • serious burn

    Stop use and ask a doctor if the condition lasts or gets worse.

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

  • Directions

    • clean the affected area
    • gently dab wound with this wipe
    • may be covered with a sterile bandage (let dry first)
  • Inactive ingredient

    purified water

  • Questions?

    1-800-841-8417 or zeemedical.com

  • SPL UNCLASSIFIED SECTION

    Distributed byZEE Medical Inc., Irvine, CA 92606

  • PRINCIPAL DISPLAY PANEL - 100 Wipe Carton

    0270

    ZEE

    FIRST AID
    ANTISEPTIC

    Helps Prevent Infection

    CLEAN
    WIPES™

    ISOPROPYL ALCOHOL WIPES
    100 Sterile Wipes
    1.2 in x 1.2 in (3.0 cm x 3.0 cm)

    Principal Display Panel - 100 Wipe Carton
  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:35418-203
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302) Isopropyl Alcohol0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:35418-203-02100 in 1 BOX
    11 mL in 1 POUCH
    2NDC:35418-203-0310 in 1 BOX
    21 mL in 1 POUCH
    3NDC:35418-203-0150 in 1 BOX
    31 mL in 1 POUCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34401/15/2013
    Labeler - ZEE MEDICAL (009645623)
    Registrant - DUKAL Corporation (791014871)
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