Label: SUKANG ALCOHOL PREP PADS MEDIUM - alcohol liquid 

  • Label RSS
  • NDC Code(s): 22408-000-01, 22408-000-02
  • Packager: Taizhou Kanglin Health Protection Products Co Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 02/13

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

  • SUKANG Alcohol Prep Pads Medium
  • Active Ingredient

    Isopropyl Alcohol, 70% v/v

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  • Purpose

    Antiseptic

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  • Uses

    Antiseptic cleanser for preparation of skin prior to an injection.

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  • 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.
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  • Directions

    Wipe injection site vigorously and discard.


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  • Other Information

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

    water

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  • SUKANG Alcohol Prep Pads Medium 100 count (22408-000-01) | SUKANG Alcohol Prep Pads Medium 200 count (22408-000-02)
  • INGREDIENTS AND APPEARANCE
    SUKANG ALCOHOL PREP PADS MEDIUM 
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:22408-000
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 70 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:22408-000-01 100 in 1 BOX
    1 0.45 g in 1 PACKET
    2 NDC:22408-000-02 200 in 1 BOX
    2 0.45 g in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333E 02/13/2013
    Labeler - Taizhou Kanglin Health Protection Products Co Ltd (530576131)
    Registrant - Taizhou Kanglin Health Protection Products Co Ltd (530576131)
    Establishment
    Name Address ID/FEI Business Operations
    Taizhou Kanglin Health Protection Products Co Ltd 530576131 manufacture(22408-000)
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