ALLURE CHEMICALS HAND WASH- benzalkonium chloride liquid

ALLURE CHEMICALS HAND WASH by

Drug Labeling and Warnings

ALLURE CHEMICALS HAND WASH by is a Otc medication manufactured, distributed, or labeled by Allure Chemicals LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.7%

Purpose

Antibacterial

Use[s]

Hand wash to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use: on children less than 2 month of age and open skin wounds.

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

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

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

Directions

*Place enough product on hands to cover all surfaces. Rub hands thoroughly with warm water for 30 seconds.

*Supervise children under 6 years of age when using this product to avoid swallowing.

*Store between 15-30° (59-86 °F)

*Avoid freezing and excessive heat above 40°C (104 °F)

Inactive Ingredients:

Ticacel, Glycerin, Distilled water, and Fragrance.

SPL UNCLASSIFIED SECTION

MEDICAL GRADE

KILLS 99.99% CORONAVIRUS AND BACTERIA IN 30 SECONDS

Manufactured and Packaged by

ALLURE Chemicals

9820-C Railroad Drive

EI Paso, Texas 79924

www.allurechemicals.com

MADE IN USA

Packaging

INGREDIENTS AND APPEARANCE

ALLURE CHEMICALS HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78804-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.7 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78804-000-94	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/25/2021
2	NDC: 78804-000-97	1890 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/25/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/25/2021

Labeler - Allure Chemicals LP (080442496)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Chemicals LP		080442496	manufacture(78804-000)