Active ingredient

8% Povidone-Iodine w/w (minimum Available Iodine 0.5%)

Purpose

Surgical Hand Scrub

Use

preoperative cleaning of healthcare personnel arms and hands. Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery.

Warnings

For external use only.

Do not use if redness or irritation occurs.

When using this product avoid contact with eyes.

Stop use and ask a doctor if severe adverse reactions occur.

Keep out of reach of children. If swallowed or gets in eyes, get medical help or contact a Poison Control Center immediately.

Directions

Clean under nails with nail pick
Wet hands and forearms
Scrub thoroughly for 3 minutes paying particular attention to the nails, cuticles and interdigital spaces
Rinse thoroughly
Repeat scrub for 3 more minutes
Rinse thoroughly

Other information

avoid excessive heat 40°C (104°F)
discard after single use.

Inactive ingredients

copper sulfate, hydrochloric acid, nonoxynol-9, sodium hydroxide, sodium nitrite, USP water.

Questions?

1-800-453-4538 Monday to Friday, 8 a.m. to 5 p.m. MST

Principal Display Panel – Carton Label

BD E-Z Scrub TM 245

Surgical Scrub Brush/Sponge
With Povidone-Iodine
and Nail Cleaner

Povidone Iodine

(minimum available Iodine 0.5%)

CONTAINS:

NOTE: SEE BACK PANEL
FOR EASY INSTRUCTIONS

Remove to check level of contents.

Reorder When Brushes Reach This Level.

REF 372453

NDC 17271-245-03

BD E-Z SCRUB
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:17271-245
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CUPRIC SULFATE ANHYDROUS (UNII: KUW2Q3U1VV)
HYDROCHLORIC ACID (UNII: QTT17582CB)
NONOXYNOL-9 (UNII: 48Q180SH9T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM NITRITE (UNII: M0KG633D4F)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:17271-245-03	10 in 1 BOX	06/01/1995	02/28/2023
1		30 in 1 CARTON
1		11 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	06/01/1995	02/28/2023

Labeler - Becton Dickinson and Company (124987988)

Name	Address	ID/FEI	Business Operations
Establishment
Becton Dickinson and Company		124987988	manufacture(17271-245) , analysis(17271-245) , label(17271-245) , pack(17271-245)

Revised: 11/2023

Document Id: 0b423ec6-c5ee-b9ae-e063-6294a90a4055

Set id: 27c96a14-63b2-47dc-8751-eb7b185facfa

Version: 6

Effective Time: 20231128

Becton Dickinson and Company