ALLAPURE ADVANCED FORMULA HAND SANITIZER- benzalkonium chloride liquid

Allapure Advanced Formula Hand Sanitizer by

Drug Labeling and Warnings

Allapure Advanced Formula Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Allapure, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose

Antiseptic/Hand & Skin Sanitizer

Uses:

Allapure *Advanced Hand Sanitizer & Wound Care is revolutionary wound care and disease protection. It helps decrease bacteria on the skin from cuts, lacerations, incisions and abrasions. Allapure* Advanced Hand Sanitizer & Wound Care promotes healing and is gentle on delicate wound tissue. Recommended for repeated use.

Warnings:

Do not freeze. For external use only.

Do not use

in ears, eyes or mouth.

When using this product, 

avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor 

if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children should be supervised when using this product.

Directions:

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Repeat if neccesary.

Inactive Ingredients:

1-Octadecyldimethyl(3-Triethoxysilylpropyl) ammonium chloride, Aloe Barbadensis leaf extract, Aqua, C12-C15 Pareth 12, Caprylyl Glucoside, Polyhexanide, Phenoxyethanol, Triethanolamine.

Questions?

+1 877.680.5758, Mon-Fri 9:00AM-5:00PM (PST)

Allapure Advanced Formula Hand Sanitizer 1.7oz (

72552-001-01)

Allapure Advanced Formula Hand Sanitizer 7oz (

72552-001-07)

Allapure Advanced Formula Hand Sanitizer 8.25oz (

72552-001-08)

INGREDIENTS AND APPEARANCE

ALLAPURE ADVANCED FORMULA HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72552-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
C12-15 PARETH-12 (UNII: 131316X18L)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72552-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/24/2018
2	NDC: 72552-001-07	207 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/24/2018
3	NDC: 72552-001-08	245 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/24/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/24/2018

Labeler - Allapure, LLC (081227305)