BD E-Z SCRUB- povidone-iodine solution

BD E-Z Scrub by

Drug Labeling and Warnings

BD E-Z Scrub by is a Otc medication manufactured, distributed, or labeled by Becton Dickinson and Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Povidone-lodine 6.5% w/w (minimum available Iodine 0.5%)

Purpose

Antiseptic

Uses

• surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care
• healthcare personnel handwash: helps reduce bacteria that potentially can cause disease

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 right away.

Directions

Surgical Hand Scrub

• Wet hands and forearms with warm water
• Use nail cleaner and then apply solution from the sponge side to work up a lather
• Scrub thoroughly for 3 minutes: difficult areas (interdigital space and fingers) with brush side, hands and forarms with sponge side
• Rinse thoroughly with warm water
• Repeat scrub for 3 minutes, sponge side only
• Rinse hands and arms thoroughly
• Dry thoroughly

Health Care Personnel Handwash

• Dispense about 5 ml of foam solution into cupped hands
• Wash in a vigorous manner covering all surfaces for 30 seconds
• Rinse thoroughly with running water (30 seconds)

Other information

avoid excessive heat above 104°F (40°C)

Inactive ingredients

ammonium nonoxynol sulfate, disodium phosphate, hydrogen peroxide, octoxynol, phosphoric acid, sodium hydroxide, water

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

PRINCIPAL DISPLAY PANEL

Principal Display Panel – Bottle Label

BD E-Z Scrub™
0.5% Povidone
Iodine Antiseptic
Solution

REF 372405 NDC: 17271-503-01

Foreign Patents and Patents Pending. U.S. Patents Pending.
U.S. Patents 6,053,369 - 6,308,866

32 FL. OZ (946 ml)

Povidone-Iodine

INGREDIENTS AND APPEARANCE

BD E-Z SCRUB 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17271-503
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ammonium nonoxynol-4 sulfate (UNII: 9HIA70O4J0)
sodium phosphate, dibasic, dihydrate (UNII: 94255I6E2T)
hydrogen peroxide (UNII: BBX060AN9V)
octoxynol 9 (UNII: 7JPC6Y25QS)
phosphoric acid (UNII: E4GA8884NN)
sodium hydroxide (UNII: 55X04QC32I)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17271-503-01	6 in 1 BOX	04/01/2000
1		946 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2000

Labeler - Becton Dickinson and Company (124987988)

Establishment
Name	Address	ID/FEI	Business Operations
Becton, Dickinson and Company		124987988	LABEL(17271-503)

Establishment
Name	Address	ID/FEI	Business Operations
Xttrium		007470579	MANUFACTURE(17271-503)