Label: SUKANG ALCOHOL PREP PADS MEDIUM- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 February 13, 2013

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  • SUKANG Alcohol Prep Pads Medium


  • Active Ingredient

    Isopropyl Alcohol, 70% v/v

  • Purpose

    Antiseptic

  • Uses

    Antiseptic cleanser for preparation of skin prior to an injection.

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    • with electrocautery procedures
    • in the eyes
    Stop use and ask a doctor if
    • irritation and redness develops
    • if condition persists for more than 72 hours, consult a physician

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    Wipe injection site vigorously and discard.

  • Other Information

    • Store at room temperature 15 degrees - 30 degrees C (59 degrees-86 degrees F)
    • Avoid excessive heat
  • Inactive Ingredient

    water

  • SUKANG Alcohol Prep Pads Medium 100 count (22408-000-01) | SUKANG Alcohol Prep Pads Medium 200 count (22408-000-02)


    AlcoholPrep200


    AlcoholPrep100


    AlcoholPrepPad

  • INGREDIENTS AND APPEARANCE
    SUKANG ALCOHOL PREP PADS MEDIUM 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22408-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22408-000-01100 in 1 BOX
    10.45 g in 1 PACKET
    2NDC:22408-000-02200 in 1 BOX
    20.45 g in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333E02/13/2013
    Labeler - Taizhou Kanglin Health Protection Products Co Ltd (530576131)
    Registrant - Taizhou Kanglin Health Protection Products Co Ltd (530576131)
    Establishment
    NameAddressID/FEIBusiness Operations
    Taizhou Kanglin Health Protection Products Co Ltd530576131manufacture(22408-000)
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