NITOUCH ALCOHOL HAND SANITIZER- ethyl alcohol spray

NiTouch ALCOHOL HAND SANITIZER by

Drug Labeling and Warnings

NiTouch ALCOHOL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Kasa Trading, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredients   Ethyl Alcohol 80% (v/v)

PURPOSE

Purpose    Antiseptic

Uses

Hand Sanitizer

For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product: Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Do not inhale

   or ingest.

Do not use in children less than 2 months of age.

Stop use and ask a doctor if irritation or a rash develops.

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

Directions

Apply enough product to cover hand thoroughly.

Rub hands together, until hands feel dry. Do not rinse.

Children under 6 years of age should be supervised when using this product.

Other information

Store below 105°F (40°C). May discolor some fabrics

Avoid freezing and excessive heat above 105°F (40°C).

Inactive ingredients

Aqua (Water), Glycerine, Fragrance, Hydrogen Peroxide, CI 42090

SPL UNCLASSIFIED SECTION

For external use only

Distributed by:

Kasa Trading, LLC

4500 E. Speedway Blvd

Tucson, AZ 85712

www.kasatrading.com

Made in India

Packaging

INGREDIENTS AND APPEARANCE

NITOUCH ALCOHOL HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80437-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80437-002-01	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/08/2020

Labeler - Kasa Trading, Llc (080477332)