Home > Drugs A-Z > Scrub Care Povidone Iodine Cleansing Scrub

Scrub Care Povidone Iodine Cleansing Scrub (CareFusion 213 LLC)

Available Formats

Dosage Form Package Information Links
SOLUTION 944 mL in 1 BOTTLE (50425-010-95) Label Information
SOLUTION 236 mL in 1 BOTTLE (50425-010-97) Label Information
SOLUTION 118 mL in 1 BOTTLE (50425-010-98) Label Information
SOLUTION 3785 mL in 1 BOTTLE (50425-010-94) Label Information
SOLUTION 472 mL in 1 BOTTLE (50425-010-96) Label Information
SOLUTION 59 mL in 1 BOTTLE (50425-010-59) Label Information

Complete Scrub Care Povidone Iodine Cleansing Scrub Information

  • Active ingredient

    Povidone-iodine, USP 7.5% (0.75% available iodine)


  • Purpose

    Antiseptic


  • Uses

    • Surgical Hand Scrub: Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care.
    • Patient Preoperative Skin Preparation: for preparation of skin prior to surgery.Helps reduce bacteria that potentially can cause skin infection.
    • Antiseptic Handwash: for hand washing to reduce bacteria on skin

  • Warnings

    For external use only

    Do not use

    • in the eyes
    • on persons allergic to iodine

    Stop use and ask a doctor if
    • skin shows symptoms of irritation, sensitivity, redness, pain or swelling. If condition persists for more than 72 hours consult a doctor.
    • In case of deep puncture wounds or serious burns.

    Keep out of reach of children

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


  • Directions

    • Surgical hand scrub: clean under nails with a nail pick. Nails should be maintained with a 1 millimeter free edge; wet hands and forearms; scrub for 3 minutes with about 5 ml of scrub and a wet brush; pay particular attention to the nails, cuticles, and interdigital spaces; rinse and repeat
    • Patient Preoperative Prep: clean the area; apply solution saturated sponge; starting at the surgical site moving outward in concentric circles for a minimum of 5 minutes; blot with sterile towel; follow with application of topical solution
    • Antiseptic Handwash: wet hands and forearms; apply ample amount of solution to wet hands: wash in vigorous manner for 15 seconds; rinse and repeat

  • Other information

    • store at room temperature
    • avoid excessive heat (above 104°F/40°C)
    • protect from freezing
    • latex free

  • Inactive ingredients

    alkyl polyglucoside, citric acid, nonylphenol ethoxylate, purified water, sodium hydroxide


  • Questions?

    Call: 1-800-523-0502 Mon.-Fri. 8 AM-5 PM CST


  • Package/Label Principal Display Panel

    Cat. 29904-004

    NDA 50425-010-98

    Cat. 29904-004

    Scrub Care® 7.5%

    Povidone-iodine, Scrub

    Antiseptic

    Non-sterile Solution

    7.5% Povidone-iodine, USP

    For preparation of skin prior to surgery.

    Helps reduce bacteria that potentially can cause skin infection.

    For Single Use Only

    Manufactured for

    CareFusion

    Vernon Hills, IL 60061 USA

    51-10108

    Net Contents: 4 fl. oz. (118 ml)

    CareFusion


  • INGREDIENTS AND APPEARANCE
    SCRUB CARE POVIDONE IODINE CLEANSING SCRUB 
    povidone iodine solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50425-010
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 7.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50425-010-59 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    2 NDC:50425-010-98 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    3 NDC:50425-010-97 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    4 NDC:50425-010-96 472 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    5 NDC:50425-010-95 944 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    6 NDC:50425-010-94 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2015
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/2001
    Labeler - CareFusion 213 LLC (831684456)
    Registrant - CareFusion 2200 Inc (832696038)
    Establishment
    Name Address ID/FEI Business Operations
    Thatcher Company 041307356 manufacture(50425-010)
    Establishment
    Name Address ID/FEI Business Operations
    CareFusion 213 LLC 826496312 pack(50425-010)