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BD Persist (Becton Dickinson Infusion Therapy Systems Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION 25 PACKAGE in 1 CARTON (17271-507-02) > 7 mL in 1 PACKAGE Label Information
SOLUTION 50 PACKAGE in 1 CARTON (17271-507-01) > 2 mL in 1 PACKAGE Label Information

Complete BD Persist Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredient

    Providone-Iodine 10% (w/w)

    Ethyl Alcohol 70% (v/v)


  • Purpose

    Antiseptic

    Antiseptic


  • Uses

    • for preparation of the skin prior to percutaneous procedure
    • helps reduce bacteria that potentially can cause skin infection
    • does not contribute to skin irritation under an occlusive dressing with repeated applications
    • reduces bacteria with routine site care for up to seven days

  • Warnings

    • For external use only
    • contains alcohol which is flammable until dry

    Do not use
    • if you are allergic to povidone iodine or ethyl alcohol
    • to treat wounds or burns
    • in eyes, mucus membranes
    • on broken skin
    • with electrocautery procedures

    Stop use and ask a doctor if the insertion site becomes

    • red
    • irritated
    • swollen
    • painful
    • infected

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Directions

    • apply with friction for 30 seconds
    • allow to dry
    • do not blot or wipe away

  • Inactive ingredients

    acrylates copolymer, ethyl alcohol, isopropyl myristate, urea, water


  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel – Carton Label

    BD Persistâ„¢
    Skin Prep

    One Step Application
    One Swab Stick

    50

    Principal Display Panel – Carton Label

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel – Package Label

    BD Persistâ„¢ Skin Prep
    1 Swab Stick REF 386401 NDC 17271-507-01

    Principal Display Panel – Package Label

  • INGREDIENTS AND APPEARANCE
    BD PERSIST 
    povidone-iodine, alcohol solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:17271-507
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (iodine - UNII:9679TC07X4) POVIDONE-IODINE 85 mg  in 1 mL
    alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol 65 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    carbomer copolymer Type A (UNII: 71DD5V995L)  
    ethyl acetate (UNII: 76845O8NMZ)  
    isopropyl myristate (UNII: 0RE8K4LNJS)  
    urea (UNII: 8W8T17847W)  
    water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:17271-507-01 50 in 1 CARTON
    1 2 mL in 1 PACKAGE
    2 NDC:17271-507-02 25 in 1 CARTON
    2 7 mL in 1 PACKAGE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 02/21/1996
    Labeler - Becton Dickinson Infusion Therapy Systems Inc. (124987988)
    Establishment
    Name Address ID/FEI Business Operations
    Becton Dickinson Infusion Therapy Systems Inc. 124987988 MANUFACTURE(17271-507)