BENZALKONIUM CHLORIDE- benzalkonium chloride swab 
Professional Disposables International, Inc.

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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HYGEA BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE 10819-3740

USE

For hand washing to decrease bacteria on the skin.

PURPOSE

Antiseptic handwash

WARNINGS

  • 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.

Keep out of reach of children.

DIRECTIONS

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

OTHER INFORMATION

Lot number and expiration date can be found on back panel of packet.

INACTIVE INGREDIENTS

Aloe Barbadensis Leaf Juice, Disodium EDTA, Potassium Sorbate, PPG-2 Hydroxyethyl Cocamide, Purified Water

SPL UNCLASSIFIED SECTION

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

ACTIVE INGREDIENT

Benzalkonium Chloride, 0.13% w/w

DOSAGE

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

PRINCIPAL DISPLAY PANEL-100 COUNT

Packet

packet

Box

box

BENZALKONIUM CHLORIDE 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-3740
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10819-3740-13 mL in 1 PACKET; Type 0: Not a Combination Product01/01/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/201211/17/2023
Labeler - Professional Disposables International, Inc. (800777117)
Establishment
NameAddressID/FEIBusiness Operations
Professional Disposables International, Inc.800777117manufacture(10819-3740)

Revised: 3/2022
 
Professional Disposables International, Inc.