Label: CHLORAPREP ONE-STEP- chlorhexidine gluconate and isopropyl alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated June 22, 2021

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

  • WARNING FLAMMABLE.

    Keep away from fire or flame.

  • Active ingredients

    Chlorhexidine gluconate 2% w/v

    Isopropyl alcohol 70% v/v

  • Purposes

    Antiseptic

    Antiseptic

  • Use

    for the preparation of the patient’s skin prior to surgery. Helps to reduce

    bacteria that potentially can cause skin infection.

  • Warnings

    For external use only. Flammable, keep away from fire or flame. To reduce risk of fire, PREP CAREFULLY:

    • solution contains alcohol and gives off flammable vapors
    • avoid getting solution into hairy areas. Hair may take up to 1 hour to dry. Wet hair is flammable.
    • do not drape or use ignition source (e.g., cautery, laser) until solution is completely dry (minimum of 3 minutes on hairless skin; up to 1 hour in hair)
    • do not allow solution to pool
    • remove wet materials from prep area
  • Allergy alert:

    This product may cause a severe allergic reaction. Symptoms may include:

    • wheezing/difficulty breathing • shock • facial swelling • hives • rash

    If an allergic reaction occurs, stop use and seek medical help right away.

  • Do not use

    • on patients allergic to chlorhexidine gluconate or any other ingredient in this product

    • for lumbar puncture or in contact with the meninges

    • on open skin wounds or as a general skin cleanser

  • When using this product

    keep out of eyes, ears, and mouth. May cause serious or

    permanent injury if permitted to enter and remain. If contact occurs, rinse with cold

    water right away and contact a doctor.

  • Stop use and ask a doctor if

    irritation, sensitization, or allergic reaction occurs. These

    may be signs of a serious condition.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison

    Control Center right away.

  • Directions

    • use with care in premature infants or infants under 2 months of age.

    These products may cause irritation or chemical burns. • use in a well ventilated area

    • maximal treatment area for one applicator is approximately 4 in. x 5 in. (130 cm2)

    • remove applicator from package; do not touch sponge • hold the applicator with the

    sponge down. Pinch wings only once to activate the ampule and release the antiseptic.

    • wet the sponge by pressing and releasing the sponge against the treatment area until liquid

    is visible on the skin • completely wet the treatment area with antiseptic • dry surgical

    sites (e.g., abdomen or arm): use gentle repeated back-and-forth strokes of the sponge for

    approximately 30 seconds Allow solution to air dry for approximately 30 seconds. Do not blot

    or wipe away. • moist surgical sites (e.g., inguinal fold): use gentle repeated back-and-forth

    strokes for approximately 2 minutes. • Allow solution to air dry for approximately

    1 minute. Do not blot or wipe away. • if using an ignition source, allow the solution to

    completely dry(minimum of 3 minutes on hairless skin; up to 1 hour in hair). Do not blot

    or wipe away. • discard the applicator after a single use along with any portion of the solution

    not required to cover the prep area. It is not necessary to use the entire amount available.

  • Other Information

    • store between 15-30 oC (59-86 oF) • avoid freezing

    and excessive heat above 40 oC (104 oF)

  • Inactive Ingredient

    USP purified water

  • Questions?

    www.chloraprep.com • call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST)

  • Prinicpa Display Panel-Carton

    54365-400-32.jpg

    Principal Display Panel-Carton

    BD ChloraPrep Clear

    3 mL Applicators

    2% w/v chlorhexidine gluconate (CHG)

    and 70% v/v Isopropyl alcohol (IPA)

    Patient Preoperative Skin Preparation

    Sterile Solution

    Applicator is sterile if package is intact

    Store between 15-30 oC (59-86 oF)

    Avoid freezing and excessive heat above 40 oC (104 oF)

    0.10 fl. oz. (3 mL) each

    25 Applicators

    NDC 54365-400-32

    REF 930400

    WARNING

    FLAMMABLE

    Keep away from fire or flame

    To reduce risk of fire, PREP CAREFULLY:

    • solution contains alcohol and gives off flammable vapors
    • avoid getting solution into hairy areas. Hair may take up to 1 hour to dry. Wet hair is flammable.
    • do not drape or use ignition source (e.g., cautery, laser) until solution is completely

    dry (minimum of 3 minutes on hairless skin; up to 1 hour in

    hair) • do not allow solution to pool • remove wet materials from prep area

    Not made with natural rubber latex

    Do not reuse

    STERILE EO

    STERILE SOLUTION

    External Use Only

    Professional Use Only

    CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co.

    Made in the USA of US and imported parts. www.bd.com

  • INGREDIENTS AND APPEARANCE
    CHLORAPREP ONE-STEP 
    chlorhexidine gluconate and isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54365-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE20 mg  in 1 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54365-400-3225 in 1 CARTON05/24/2019
    11 in 1 POUCH
    13 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02083205/24/2019
    Labeler - CareFusion 213, LLC (826496312)
    Registrant - CareFusion 2200, Inc (832696038)
    Establishment
    NameAddressID/FEIBusiness Operations
    CareFusion 213, LLC826496312analysis(54365-400) , label(54365-400) , manufacture(54365-400) , pack(54365-400)