PURELOGIC ANTIBACTERIAL HAND WIPES REFRESHING SINGLE TO GO PACKS- benzalkonium chloride solution

PureLogic Antibacterial Hand Wipes Refreshing Single To Go Packs by

Drug Labeling and Warnings

PureLogic Antibacterial Hand Wipes Refreshing Single To Go Packs by is a Otc medication manufactured, distributed, or labeled by Argento sc by sicura inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.2%

PURPOSE

Purpose: 

Disinfectant

USE

Decrease bacteria on skin that could cause disease

Recommended for repeated use

warnings

For external use only on hands. Flammable, keep way from flame or fire

When using this product

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not ingest or inhale

Avoid contact with broken skin

stop use and ask a doctor

if irrigation and redness develop and condition persists for more than 72 hours

keep out of reach of children

if swallowed,get medical help or contact a Poison Control Center immediately

Directions

• Wipe product on hands thoroughly and allow to dry, do not wipe off
• For children under 6, use under adult supervision
• Not recommended for use with infants

other information

Do not store above 105F (40.6C)

May discolor some fabrics

Harmful to plastics and wood finishes

inactive ingredients

Purified water, Phenoxyethanol, Ethylhexylglycerin, Didecyldimonium Chloride, Propylene

Glycol, Glycerin, Fragrance, Aloe Barbadensis Leaf Jiuce

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELOGIC ANTIBACTERIAL HAND WIPES REFRESHING SINGLE TO GO PACKS 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77731-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.006 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77731-014-01	48 in 1 BOX	07/23/2020
1		1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/23/2020

Labeler - Argento sc by sicura inc. (168718778)