PURPLE HAND SANITIZER- benzalkonium chloride 0.13% spray

Purple Hand Sanitizer by

Drug Labeling and Warnings

Purple Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ASN Technologies Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

To help reduce bacteria that potentially can cause disease. For when soap and water are not available.

Warnings

For external use only.

Do Not Use

on open skin wounds or on children less than two months of age

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

On dry hands, place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until hands are entirely dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store between 15-30C (59-86F)
Avoid heating and temperatures above 40C (104F)

Inactive Ingredients

Silica complex 1-octadecanaminium, N,n-dimethyl-n-(3-(trihydroxysilyl)propyl) Chloride, Polyoxyethylenesorbitan monolaurate, Glycerol, Sodium Benzoate, Aqua

Purple Hand Sanitizer

INGREDIENTS AND APPEARANCE

PURPLE HAND SANITIZER 
benzalkonium chloride 0.13% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82294-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.078 g  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDE (UNII: GLJ50K866T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82294-001-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2021
2	NDC: 82294-001-40	40 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/01/2021

Labeler - ASN Technologies Inc (204344589)

Registrant - ASN Technologies Inc (204344589)