Label: PHARMACIST CHOICE ALCOHOL STERILE PREP PAD- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2024

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  • Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

  • Purpose

    Antiseptic

  • Keep out of children

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Use

    For preparation of skin prior to injection; to decrease germs in minor cuts and scrapes.

  • Warning

    For external use only. Flammable, keep away from fire and flame.

  • Directions

    Wipe injection site vigorously.

  • Inactive ingredients

    Water

  • Drug Facts

    Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

    Purpose:

    Antiseptic

    Use: For preparation of skin prior to injection; to decrease germs in minor cuts and scrapes.

    Warning: For external use only. Flammable, keep away from fire and flame.

    Keep out of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

    Caution: Don’t apply to a irritated skin.

    Don’t use in the eyes, or on mucous membranes.

    In case of deep or puncture wounds, consult a doctor.

    Directions: wipe injection site vigorously.

    Other information: Store at room temperature.

    Inactive ingredients: Water

    Labeling of carton

  • INGREDIENTS AND APPEARANCE
    PHARMACIST CHOICE ALCOHOL STERILE PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62379-005
    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)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62379-005-051.4 mL in 1 POUCH; Type 0: Not a Combination Product10/10/2017
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/23/2015
    Labeler - Simple Diagnostics (004135503)
    Registrant - Simple Diagnostics (004135503)
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