Drug Labeling and Warnings

Drug Details [pdf]

BD E-Z CARE- alcohol 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.

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Drug Facts

Active ingredient

Ethyl alcohol 70% w/w

Purpose

Antiseptic

Uses

  • Surgical hand antiseptic: Significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care.
  • Healthcare personnel hand antiseptic: Helps reduce bacteria that potentially can cause disease.

Warnings

Flammable: keep away from fire or flame. 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

Surgical Hand Antiseptic

  • Apply to clean, dry hands and nails. Clean under nails with a nail pick. Nails should be maintained with a 1 -millimeter free edge.
  • Dispense a half palmful (approximately 3.0 mL) of solution in one hand.
  • Dip the fingers of the opposite hand into the solution and work in under the nails.
  • Spread the remaining solution over the hand and up to just above the elbow. Rub thoroughly for 30 seconds or until dry, paying particular attention to the nails, cuticles and interdigital spaces.
  • Using another half palmful (approximately 3.0 mL), repeat with the other hand.
  • Dispense another half palmful (approximately 3.0 mL) of solution into either hand and reapply to all aspects of both hands up the wrists. Rub thoroughly for 30 seconds or until dry.

Healthcare Personnel Hand Antiseptic

  • Apply to clean, dry hands and nails.
  • Dispense a half palmful (approximately 3.0 mL) into the palm of one hand.
  • Spread the solution evenly to cover both hands up to the wrists, paying particular attention to the nails, cuticles and interdigital spaces. Rub hands for 15 seconds or until dry.

Other information

avoid excessive heat 40°C (104°F)

  • discard container when empty
  • suitable for use with CHG Products.

Inactive ingredients

behentrimonium methosulfate, benzalkonium chloride, benzethonium chloride, cetearyl alcohol, chlorhexidine gluconate, dimethicone, docosanol, fragrance, glycerin, isopropyl palmitate, methylparaben, mineral oil, PEG-10 behenyl ether, PEG-40 castor oil, propylparaben, stearalkonium chloride, USP water.

Questions?

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

Canada 1-800-268-5430 Monday to Friday, 8 a.m. to 4 p.m. EST

Principal Display Panel – Bottle Label

BD E-Z Care

70% Ethyl Alcohol Solution
Rinseless, Brushless Antiseptic

Surgical and Healthcare Personnel
Hand Antiseptic with Moisturizers
Suitable for use with CHG products

REF 372408
NDC: 17271-501-01 DIN 02248476
Foreign Patents and Patents Pending. U.S. Patent 6,723,689
32 FL. OZ (946 mL)

Principal Display Panel – Bottle Label
BD E-Z CARE 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 17271-501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol600 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
behentrimonium methosulfate (UNII: 5SHP745C61)  
benzalkonium chloride (UNII: F5UM2KM3W7)  
benzethonium chloride (UNII: PH41D05744)  
cetostearyl alcohol (UNII: 2DMT128M1S)  
chlorhexidine gluconate (UNII: MOR84MUD8E)  
dimethicone (UNII: 92RU3N3Y1O)  
docosanol (UNII: 9G1OE216XY)  
glycerin (UNII: PDC6A3C0OX)  
isopropyl palmitate (UNII: 8CRQ2TH63M)  
methylparaben (UNII: A2I8C7HI9T)  
mineral oil (UNII: T5L8T28FGP)  
beheneth-10 (UNII: 313S43DM16)  
polyoxyl 40 castor oil (UNII: 4ERD2076EF)  
propylparaben (UNII: Z8IX2SC1OH)  
stearalkonium chloride (UNII: 0OUO26BB88)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 17271-501-016 in 1 BOX04/01/200410/02/2015
1946 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/01/200410/02/2015
Labeler - Becton Dickinson and Company (124987988)

Revised: 2/2012