PURELOGIC FOAMING HAND SANITIZER EUCALYPTUS MINT- benzalkonium chloride solution

PureLogic Foaming Hand Sanitizer Eucalyptus Mint by

Drug Labeling and Warnings

PureLogic Foaming Hand Sanitizer Eucalyptus Mint 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 0.13%

PURPOSE

Purpose: 

Antibacterial

Use

Hand sanitizer to help reduce bacteria on skin that could cause disease

Recommended for repeated use

Warnings

For external use on hands only.

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 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 immediately

Directions

• Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry
• Children under 6 years of age should be supervised when using this product

Other information

To prevent discoloration, avoid contact with clothing

Inactive ingredients

Water, Sodium lauroamphoacetate, Cocamidopropylamine oxide, Cocamidopropyl betaine, Glycerin, Olea europaea (olive) leaf extract, Polyminopropyl biguanide, Citric acid, Disodium EDTA, Benzophenone-3, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Cetylpyridinium chloride,  Blue 1 (CI42090)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELOGIC FOAMING HAND SANITIZER EUCALYPTUS MINT 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77731-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DISODIUM HEDTA (UNII: KME849MC7A)
BENZOPHENONE (UNII: 701M4TTV9O)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77731-056-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/31/2020

Labeler - Argento sc by sicura inc. (168718778)