JANITEX ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth

JANITEX ANTIBACTERIAL WET WIPES by

Drug Labeling and Warnings

JANITEX ANTIBACTERIAL WET WIPES by is a Otc medication manufactured, distributed, or labeled by Pacific Health Systems Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

JANITEX ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79519-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79519-021-01	160 in 1 CANISTER	09/18/2020
1		3 g in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/18/2020

Labeler - Pacific Health Systems Inc. (080638960)