JANITEX ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth 
Pacific Health Systems 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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JANITEX Antibacterial Wet Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1 %

Purpose

Antiseptic Hand Cleanser

Uses

Kills harmful germs

Warnings

• For external use only. Harmful if swallowed.
• When using this product, avoid contact with the eyes. If contact occurs, rinse thoroughly with water.
• Stop use and ask a doctor if irritation develops.

• Keep out of reach of children. If swallowed, call a poison control center or get medical help right away.

Directions

• Adults and children over 2 years old
• For occasional and personal domestic use
• Supervise children when they use this product
• Rub thoroughly into hands for at least 30 seconds. Allow to dry

Inactive Ingredients

Aqua, Sodium Benzoate, Phenoxyethanol, Parfum, Benzoic Acid, Dehydroacetic Acid, Panthenol, Sodium Cocoamphoacetate, Sodium Lauriminodipropionate, Octyldodecanol

Other Informations

Store in a cool & dry place

Questions?

+1 (862) 318-4763

ANTIBACTERIAL

Ultra Protection

pH 5.5

E Vitamin

DERMATOLOGICALLY TESTED

+ Moisturizer

Non-Woven Fabric

Bleach Free

Distributed by Pacific Health Systems Inc.

19 Commerce Road Unit E Fairfield, NJ 07004

info@janitexus.com www.janitexus.com

STORAGE AND DISPOSAL

• Do not leave canisters open during storage

• Do not reuse wipe

• Dispose of used wipe in trash

• Do not reuse or refill canister. Offer for recycling if available

Made in Turkey

Packaging

IMAGE

JANITEX ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79519-021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
PANTHENOL (UNII: WV9CM0O67Z)  
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
SODIUM LAURIMINODIPROPIONATE (UNII: 7G447D0DH9)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79519-021-01160 in 1 CANISTER09/18/2020
13 g in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/18/2020
Labeler - Pacific Health Systems Inc. (080638960)

Revised: 9/2020
Document Id: 610f4eb9-e248-46f9-a28b-179aca6d9fed
Set id: 8ba8c1f9-92da-4d88-911b-1423c1ab451b
Version: 1
Effective Time: 20200918
 
Pacific Health Systems Inc.