JANITEX 75% ALCOHOL WET WIPES- ethyl alcohol cloth

JANITEX by

Drug Labeling and Warnings

JANITEX 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

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

For hand sanitizing to decrease bacteria and germs on skin.

Apply topically to the skin to help prevent cross contamination.

Dries in seconds.

Warnings

For external use only. Harmful if swallowed.

Do not use as baby wipes.

Do not flush down the toilet. 

Do not use in or contact the eyes.  

Do Not Use

Highly flammable. Keep away from fire or flame.

Do not eat or drink when handling

 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

 Lift the tab on the top of the lid to open.

 Open moisture seal film package before use.

 Pull out first wipe through the dispensing center of the canister.

Next sheets pops up automatically

 Close the lid to retain moisture.

 Wipe clean with this product. Let air dry

Other Informations

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

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

INACTIVE INGREDIENT

Inactive Ingredients Aqua, Glycerin, Parfum

SPL UNCLASSIFIED SECTION

ANTIVIRUS

ANTI - FUNGAL

Kills 99.9% Bacteria & Germs

FDA

75% Alcohol Concentration

99.9% Efficient Sterilization

Non-Woven Skin

Moisturizes and Doet Not Dry

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  75% ALCOHOL WET WIPES
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79519-020
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79519-020-03	40 in 1 PACKET	06/30/2020
1		4.16 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 79519-020-02	60 in 1 BOX	06/30/2020
2		4.16 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 79519-020-01	80 in 1 CANISTER	06/30/2020
3		4.16 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC: 79519-020-04	80 in 1 CANISTER	09/01/2020
4		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)