SCRUB CARE POVIDONE IODINE CLEANSING SCRUB- povidone iodine solution 
CareFusion 213 LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Scrub Care® Povidone Iodine Cleansing Scrub

Active ingredient

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

Purpose

Antiseptic

Uses

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

Other information

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

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)

Revised: 10/2016
Document Id: 3eb19bcf-a9da-31d7-e054-00144ff8d46c
Set id: 19182492-4cde-481f-bac0-7b47ac8cad4e
Version: 6
Effective Time: 20161012
 
CareFusion 213 LLC