Label: ISOPROPYL ALCOHOL swab

  • NDC Code(s): 8290-3268-95
  • Packager: Becton Dickinson and Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 2, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Isopropyl Alcohol, 70% v/v

  • Purpose

    Antiseptic

  • Use

    for the preparation of skin prior to an injection to decrease germs in minor cuts and scrapes.

  • Warning:

    • For External use only. FLAMMABLE, keep away from fire or flame.

    Keep out of the reach of children.

    If swallowed, get medical help or contact a poison control center immediately.

    Caution do not apply to irritated skin.

    Do not use in the eyes, or on mucous membranes.

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

    Discontinue use if irritation and redness develops. If condition persists for more than 72 hours, consult a doctor.

  • Directions

    wipe injection site vigorously.

  • Other Information

    store at room temperature.

  • Inactive Ingredient

    water.

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel – Carton Label.

    NDC/HRI# 08290-3268-95

    326895

    100 Swabs

    BD Alcohol Swabs

    Antiseptic for preparation of the skin prior to injection

    CALL: 1.888.BDCARES (1.888.232.2737)

    VISIT: www.bd.com/us/diabetes

    WRITE: BD, 1 Becton Drive, Franklin Lakes, NJ 07417

    Principal Display Panel – Carton Label
  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:8290-3268
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302) Isopropyl Alcohol0.75 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:8290-3268-9512 in 1 CARTON10/01/1993
    1100 in 1 BOX
    11 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/01/1993
    Labeler - Becton Dickinson and Company (001292192)
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