JANITEX DISINFECTING WIPES 75% ALCOHOL- ethyl alcohol cloth

JANITEX DISINFECTING WIPES 75% ALCOHOL by

Drug Labeling and Warnings

JANITEX DISINFECTING WIPES 75% ALCOHOL 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

Ethyl Alcohol 75 %

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 container plastic cover. Tear off moisture seal film. Pull out wipe corner from the center of wipe roll; twist wipe corner through the dispensing center of the canister. Next sheets pop up automatically. Keep center cap 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, Glycerin, Propylene Glycol, Parfum, Tocopheryl Acetate, Citric Acid, Aloe Barbadensis Extract

SPL UNCLASSIFIED SECTION

75% Alcohol

75% Alcohol Concentration

E Vitamin 

+ moisturizer

non-woven fabric

Bleach Free

Ultra Protection

DISINFECTING WIPES

Distributed by Pacific Health Systems Inc.

19 Commerce Road Unit E Fairfield, NJ 07004

info@janitexus.com www.janitexus.com

Made in Turkey

Packaging

INGREDIENTS AND APPEARANCE

JANITEX DISINFECTING WIPES 75% ALCOHOL 
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79519-060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79519-060-01	80 in 1 CANISTER	08/11/2020
1		1.83 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)