ALLURE HAND WASH- benzalkonium chloride liquid

Allure Hand Wash by

Drug Labeling and Warnings

Allure Hand Wash by is a Otc medication manufactured, distributed, or labeled by Allure Chemicals LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drugs Facts

Active ingredient

Benzalkonium chloride 0.7%

Purpose

Antibacterial

Uses [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: in children less than 2 months 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  doctor if irritation or rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact 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.

Storage

Store between 15-30°C (59-86 °F)

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

Inactive Ingredients:

Distilled water, Polyglyceryl-10 Hexaoleate, Na EDTA, Decyl Glucoside, Sodium Cocoamphoacetate, Fragrances, Vitamin E acetate, Phenoxyethanol, Alpha-Cyclodextrin, Aloe Extract, Citric

SPL UNCLASSIFIED SECTION

ALLURE CHEMICALS INSTANT HAND WASH

MEDICAL GRADE

KILLS 99.9% OF GERMS, COLD AND FLU VIRUSES

Manufactured and Packaged by
Allure Chemicals
9820-C Railroad Drive
El Paso Texas 79924
www.allurechemicals.com

MADE IN USA

Packaging

INGREDIENTS AND APPEARANCE

ALLURE HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78804-898
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	7 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYGLYCERYL-10 HEXAOLEATE (UNII: 8S25IPV09I)
EDETATE SODIUM (UNII: MP1J8420LU)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALFADEX (UNII: Z1LH97KTRM)
ALOE (UNII: V5VD430YW9)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78804-898-08	0.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/04/2021
2	NDC: 78804-898-16	0.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/04/2021
3	NDC: 78804-898-32	0.946 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/04/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/04/2021

Labeler - Allure Chemicals LP (080442496)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Chemicals LP		080442496	manufacture(78804-898)