BD E-Z SCRUB- chloroxylenol solution 
Becton Dickinson and Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

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

Other information

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 – Carton Label

BD

BD E-Z Scrub116

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

Principal Display Panel – Carton Label
BD E-Z SCRUB 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17271-116
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17271-116-0310 in 1 BOX03/01/1989
130 in 1 CARTON
116 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/1989
Labeler - Becton Dickinson and Company (124987988)
Establishment
NameAddressID/FEIBusiness Operations
Becton Dickinson and Company124987988manufacture(17271-116) , analysis(17271-116) , label(17271-116) , pack(17271-116)

Revised: 5/2022
Document Id: df4e0622-3cf0-5cec-e053-2a95a90ac345
Set id: 5a094bb7-5648-4538-abd2-70d3a61af6f2
Version: 4
Effective Time: 20220518
 
Becton Dickinson and Company