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

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

BD E-Z Scrub 245 TM

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

Povidone Iodine

(minimum available Iodine 0.5%)

CONTAINS:

30

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

INGREDIENTS AND APPEARANCE

BD E-Z SCRUB 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17271-245
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
cupric sulfate anhydrous (UNII: KUW2Q3U1VV)
hydrochloric acid (UNII: QTT17582CB)
nonoxynol-9 (UNII: 48Q180SH9T)
sodium hydroxide (UNII: 55X04QC32I)
sodium nitrite (UNII: M0KG633D4F)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17271-245-03	10 in 1 BOX	06/01/1995
1		30 in 1 CARTON
1		11 mL in 1 PACKAGE; 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	06/01/1995

Labeler - Becton Dickinson and Company (124987988)

Establishment
Name	Address	ID/FEI	Business Operations
Becton, Dickinson and Company		124987988	MANUFACTURE(17271-245)

Establishment
Name	Address	ID/FEI	Business Operations
Thatcher		041307356	MANUFACTURE(17271-245)