Label: ALCOHOL PREP- isopropyl alcohol swab

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

Drug Label Information

Updated November 17, 2023

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  • Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

  • Purpose

    Antiseptic

  • Uses

    • To prepare skin prior to injection
    • To decrease germs in minor cuts and scrapes
  • Warnings

    For external use only

    Flammable. Keep away from fire or flame

    Do not use

    • with electrocautery procedures
    • in the eyes
    • on mucous membranes
    • on irritated skin

    Stop use and ask doctor if

    • irritation or redness develops
    • if condition persists for more than 72 hours

    Caution

    In case of deep or puncture wounds, consult a doctor

    Keep out of reach of children

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

  • Directions for use

    • wipe injection site vigorously and discard
  • Other Information

    • Store at room temperature 59-86⁰F (15-30⁰C)
    • Avoid excessive heat
  • Inactive Ingredient

    purified water

  • Principal Display Panel

    NDC 70000-0112-1

    LEADER

    Alcohol Swabs

    70% Isopropyl Alcohol

    STERILE

    Antiseptic for Preparation of Skin Prior to Injection

    Latex Free

    Extra Thick

    Individually Wrapped Packets

    COMPARE TO BD ALCOHOL SWABS

    active ingredients*

    100% Money Back Guarantee

    100 SWABS

    Label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0112-140 in 1 CASE06/22/2016
    1100 in 1 BOX
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/21/2016
    Labeler - Cardinal Health (063997360)
    Registrant - Phoenix Innovative Healthcare Manufacturers Private Limited (650743854)
    Establishment
    NameAddressID/FEIBusiness Operations
    Phoenix Innovative Healthcare Manufacturers Private Limited650743854manufacture(70000-0112)