Label: CUT CARE ALCOHOL PREP PAD- isopropyl alcohol swab 

  • Label RSS
  • NDC Code(s): 53439-100-01, 53439-100-10
  • Packager: Zeus Medical Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 09/13

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

  • Active ingredient

    Isopropyl alcohol 70% v/v

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  • Purpose

    Antiseptic

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  • Use

    For preparation of the skin prior to injection

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  • Warnings

    • For external use only
    • Flammable, keep away from flame or fire
    • Not for use with electrocautinary devices or procedures
    • Do not use in eyes
    • Sterile unless package is damaged or open.

    Stop use and ask a doctor if:

    • Irritation or redness develops
    • condition persists for more than 72 hours

    Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

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  • Directions

    • Wipe injection site vigorously and discard
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  • Other information

    store at room temperature: 15 - 30C (59F – 86F)

    • avoid excessive heart
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  • Inactive Ingredient

    purified water

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  • PRINCIPAL DISPLAY PANEL

    NDC 53439-100-10
    Cut Care

    Alcohol Prep Pad

    Saturated with 70% Isopropyl Alcohol

    Contents: 100 Pouches

    PRINCIPAL DISPLAY PANEL
NDC 53439-100-10
Cut Care
Alcohol Prep Pad
Saturated with 70% Isopropyl Alcohol
Contents: 100 Pouches

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  • INGREDIENTS AND APPEARANCE
    CUT CARE ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:53439-100
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 0.7 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53439-100-10 100 in 1 CARTON
    1 NDC:53439-100-01 1 in 1 POUCH
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333A 09/15/2013
    Labeler - Zeus Medical Holdings LLC (014884052)
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