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

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Drug Facts

Active ingredient

Chloroxylenol (PCMX) 3% w/w

Purpose

Antiseptic

Uses

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

Health Care Personnel Hand Wash

Other information

store between 68-77°F (20-25°C)

Inactive ingredients

aloe vera, disodium laurethsulfosuccinate, fragrance, FD&C green #3, D&C yellow #10, lanolin, poloxamer, propylene glycol, sodium cocoyl isethionate, sodium lauryl ether sulfate, water

Questions?

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

Principal Display Panel – Bottle Label

BD E-Z Scrub™
3% Chloroxylenol
Antiseptic Solution

REF 372404 • NDC 17271-502-01

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

32 FL. OZ (946 ml)

3% PCMX

Principal Display Panel – Bottle Label
BD E-Z SCRUB 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17271-502
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
LANOLIN (UNII: 7EV65EAW6H)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
POLOXAMER 184 (UNII: BIS92ZSF57)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17271-502-016 in 1 BOX04/01/2000
1946 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:17271-502-026 in 1 BOX04/01/200010/31/2016
2946 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)04/01/2000
Labeler - Becton Dickinson and Company (124987988)

Revised: 11/2023
Document Id: 0b6a66a9-b8cc-ebfe-e063-6294a90a09f8
Set id: 471afae4-336b-4707-9293-563333e515e3
Version: 6
Effective Time: 20231130
 
Becton Dickinson and Company