BD E-Z SCRUB- chloroxylenol 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

3% (512mg) Chloroxylenol (PCMX) w/w

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

cellulose, fragrance, hydrochloric acid, lanolin, nonoxynol-4, propylene glycol, sodium hydroxide, sodium lauryl sulfosuccinate, water.

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

PRINCIPAL DISPLAY PANEL

Principal Display Panel – Carton Label

BD

BD E-Z Scrub™ 116

Surgical Scrub Brush/Sponge
With 3% Chloroxylenol,
Emollients and Nail Cleaner

3% PCMX

CONTAINS:
30

NOTE: SEE BACK PANEL
FOR EASY INSTRUCTIONS

Remove to check level of contents

Reorder When Brushes Reach This Level.

REF 371163

NDC: 17271-116-03

REMOVE FOR CONVENIENT DISPENSING OF PRODUCT SEE REVERSE SIDE FOR EASY MOUNTING INSTRUCTIONS

INGREDIENTS AND APPEARANCE

BD E-Z SCRUB 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17271-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
chloroxylenol (UNII: 0F32U78V2Q) (chloroxylenol - UNII:0F32U78V2Q)	chloroxylenol	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
powdered cellulose (UNII: SMD1X3XO9M)
hydrochloric acid (UNII: QTT17582CB)
lanolin (UNII: 7EV65EAW6H)
nonoxynol-4 (UNII: KND68343W4)
propylene glycol (UNII: 6DC9Q167V3)
sodium hydroxide (UNII: 55X04QC32I)
disodium lauryl sulfosuccinate (UNII: P160Q81342)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17271-116-03	10 in 1 BOX	03/01/1989
1		30 in 1 CARTON
1		16 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	03/01/1989

Labeler - Becton Dickinson and Company (124987988)

Establishment
Name	Address	ID/FEI	Business Operations
Becton Dickinson and Company		124987988	MANUFACTURE(17271-116)

Establishment
Name	Address	ID/FEI	Business Operations
Thomas Swan & Co. Ltd.		212082770	MANUFACTURE(17271-116)