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 Ingredients

Benzalkonium Chloride (0.1%)

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin that could cause disease

Warnings

• For external use only, harmful if swallowed.
• Do not use as baby wipe.
• Do not flush.
• Do not use on open skin wounds.
• Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or allergic reaction occurs.
• Flammable - Keep away from fire or flame

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

Directions

Open lid, gently peel back resealable label, remove and use wipes as required. Keep lid closed to prevent moisture loss.

No need to rinse after usage. Allow skin to dry without wiping. For adults and children 2 years and over. Discard properly after use. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store in dry and cool place and away from oxidizers.

Inactive ingredients

Aqua, Phenoxyethanol, Propylene Glycol, Parfum, Cocamidopropyl Betaine, PEG-40 Hydrogenated Castor Oil, Benzoic Acid, Tetrasodium EDTA, Dehydroacetic Acid, Sodium Hydroxide

SPL UNCLASSIFIED SECTION

pH 5.5

E Vitamin

DERMATOLOGICALLY TESTED 

+ moisturizer 

non-woven fabric

Bleach Free

Ultra Protection

ANTIBACTERIAL

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: 79519-050
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)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79519-050-01	90 in 1 PACKET	08/11/2020
1		3.23 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	08/11/2020

Labeler - Pacific Health Systems Inc. (080638960)