PDI Benzalkonium Chloride Antiseptic Towelettes

Dosage form: cloth
Ingredients: Benzalkonium Chloride 0.13mL in 1mL
Labeler: Professional Disposables International, Inc.
NDC Code: 10819-3737

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.

PDI BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTES

UseFor hand washing to decrease bacteria on the skin

Warnings
  • Flammable, keep away from fire or flame.
  • For external use only.
  • If swallowed, get medical help or contact a Poison Control Center right away.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
  • Do not use in the eyes.

Keep out of reach of children.

Directions
  • Tear open packet.
  • Unfold and use; discard after single use.
  • Wet hands thoroughly with product and allow to dry without wiping.

Other informationLot No. and Expiration Date can be found on back panel of packet.

Dosage
Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

USP Purified Water

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
www.pdipdi.com              Made in USA

Principal Display Panel - 100 Count PDI
Benzalkonium Chloride
Antiseptic Towelettes


For Professional and Hospital Use

1 Towelette [7.7 x 5.0 in (19.6 x 12.7 cm)] 100 Towelettes per Box

Packet Label
Box Label

Active ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Antiseptic handwash

PDI BENZALKONIUM CHLORIDE  ANTISEPTIC TOWELETTES
bzk cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-3737
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (BENZALKONIUM) Benzalkonium Chloride0.13 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:10819-3737-1100 PACKET (PACKET) in 1 BOX
13.0 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1983
Labeler - Professional Disposables International, Inc. (800777117)
Establishment
NameAddressID/FEIOperations
Professional Disposables International, Inc.800777117manufacture

Revised: 05/2012
 
Professional Disposables International, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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