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, Thatcher Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

13% Povidone-lodine w/w (minimum available Iodine 1%)

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

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

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

Principal Display Panel - BD E-Z Scrub 205 Carton Label

BD

BD E-Z Scrub™ 205

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

Povidone
Iodine

(minimum available Iodine 1%)

CONTAINS:

30

NOTE: SSEE BACK PANEL
FOR EASY INSTRUCTIONS

Remove to check level of contents.

Reorder When Brushes Reach This Level.

0130382903720539

REF 372053

NDC: 17271-205-03

REMOVE FOR CONVENIENT DISPENSING OF PRODUCT

SEE REVERSE SIDE FOR EASY MOUNTING INSTRUCTIONS

INGREDIENTS AND APPEARANCE

BD E-Z SCRUB 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17271-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
povidone-iodine (UNII: 85H0HZU99M) (iodine - UNII:9679TC07X4)	iodine	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ammonium nonoxynol-4 sulfate (UNII: 9HIA70O4J0)
sodium phosphate, dibasic, monohydrate (UNII: BWZ7K44R51)
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: 17271-205-03	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(17271-205)

Establishment
Name	Address	ID/FEI	Business Operations
Thatcher Company		041307356	MANUFACTURE(17271-205)