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 (0.2%)

Purpose

Antiseptic

Uses

● For hand sanitizing to decrease bacteria and germs on skin.

● Apply topically to the skin to help prevent cross contamination.

● Not Recommended for repeated use.

● Dries in seconds.

Warnings

For external use only. Harmful if swallowed.

Do not use as baby wipes.

Do not use in or contact the eyes.

Avoid contact with open or exposed wounds.

When Using

Keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water

Stop Use

Stop use if too much skin irritation and sensitivity develops or increases

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

● Open lid, gently peel back resealable label, remove and use wipes as required

● Reseal after use to avoid evaporation of alcohol it is a violation of federal law to use this product in

a manner inconsistent with its labeling.

Other Informations

Store at room temperature 15-30℃ (59-86°F).

Lot No. Manufacture date and expiration date can be found on package.

Inactive Ingredients

Aqua, Olus Oil, Glycerin, Lauryl Glucoside, Polyglyceryl-2- Dipolihydroxystearate, Glyceryl Oleate,

Dicapiryl Carbonate, Perfume, Triethanolamine

SPL UNCLASSIFIED SECTION

Kills 99.9% Bacteria & Germs

ANTIBACTERIAL

ANTI - FUNGAL

pH 5.5

BLEACH FREE

Made in Turkey

Distributed by Pacific Health Systems Inc.

19 Commerce Road Unit E Fairfield, NJ 07004

info@janitexus.com    www.janitexus.com

Packaging

INGREDIENTS AND APPEARANCE

JANITEX ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79519-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CORN OIL (UNII: 8470G57WFM)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
GLYCERYL OLEATE (UNII: 4PC054V79P)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79519-010-01	72 in 1 CARTON	06/30/2020
1		4.16 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 79519-010-02	80 in 1 CARTON	06/30/2020
2		4.16 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 79519-010-03	100 in 1 CARTON	06/30/2020
3		4.16 mL 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	06/30/2020

Labeler - Pacific Health Systems Inc. (080638960)