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

  • DEA Schedule: None
  • Marketing Status: New Drug Application

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/13

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

  • Active ingredients

    Chlorhexidine gluconate 2% w/v

    Isopropyl alcohol 70% v/v

  • Purposes



  • Use

    for the preparation of the patient's skin prior to surgery. Helps to reduce bacterial that potentially can cause skin infection.

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame. To reduce the 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

    Do not use

    on patients with known allergies to chlorhexidine gluconate or isopropyl alcohol
    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 8.4 in. x 8.4 in. (457 cm 2)
    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 back-and-forth strokes for 30 seconds
    moist surgical sites (e.g., inguinal fold): use gentle back-and-forth strokes for 2 minutes
    do not allow the solution to pool; tuck prep towels to absorb solution, and then remove
    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 °C (59-86 °F)
    avoid freezing and excessive heat above 40 °C (104 °F)
    the tint will slowly fade from the skin. Soap and water, or alcohol may be used to remove the tint if desired.
  • Inactive ingredients

    FD&C green #3 dye
    USP purified water
  • Questions?
    call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST)
  • Package/Label Principal Display Panel

    Carton Front Panel, 10.5ml Teal

    10.5ml Teal Carton Primary Display Panel

    10.5ml Teal Carton Primary Display Panel


    NDC 054365-400-09

    10.5ml APPLICATORS

    Scrub Teal®

    Not made with natural rubber latex

    Applicator is sterile if package is intact

    Professional Use Only

    Store between 15-30 °C (59-86 °F)

    Avoid freezing and excessive heat above 40 °C (104 °F)

    25 applicators

    0.36 fl. oz. (10.5 ml) each

    chlorhexidine gluconate and isopropyl alcohol solution
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:54365-400
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Inactive Ingredients
    Ingredient Name Strength
    FD&C GREEN NO. 3  
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54365-400-09 25 in 1 CARTON
    1 1 in 1 POUCH
    1 10.5 mL in 1 APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA020832 04/26/2002
    Labeler - CareFusion 213 LLC (826496312)
    Registrant - CareFusion 2200, Inc (832696038)
    Name Address ID/FEI Business Operations
    CareFusion 213 LLC 826496312 ANALYSIS(54365-400), MANUFACTURE(54365-400), LABEL(54365-400), PACK(54365-400)