PURACY NATURAL FOAMING HAND SANITIZER- benzalkonium chloride solution

Puracy Natural Foaming Hand Sanitizer by

Drug Labeling and Warnings

Puracy Natural Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Puracy LLC, Bayscience Formulators, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium Chloride 0.1%

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses

for hand sanitizing to decrease bacteria on the skin

recommended for repeated use

WARNINGS

Warnings

For external use only

When using this product avoid contact with eyes.

In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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

DOSAGE & ADMINISTRATION

Directions

pump a small amount of foam into palm of hand

rub thoroughly over all surfaces of both hands

rub hands together briskly until dry

INACTIVE INGREDIENT

Inactive ingredients

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid

PRINCIPAL DISPLAY PANEL

puracy

NATURAL FOAMING

HAND SANITIZER

alcohol-free   kills 99.9% of germs

FRAGRANCE FREE

Austin Texas   8.5 fl.oz. (251 mL)

INGREDIENTS AND APPEARANCE

PURACY NATURAL FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72905-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72905-001-08	251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/20/2019
2	NDC: 72905-001-05	18927 mL in 1 PAIL; Type 0: Not a Combination Product	02/20/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/20/2019

Labeler - Puracy LLC (079535215)

Establishment
Name	Address	ID/FEI	Business Operations
Bayscience Formulators, LLC		162930544	manufacture(72905-001)