PURELOGIC EUCALYPTUS ANTIBACTERIAL HAND- benzalkonium chloride soap

PureLogic Eucalyptus Antibacterial Hand by

Drug Labeling and Warnings

PureLogic Eucalyptus Antibacterial Hand 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

Helps eliminate bacteria on hands

Warnings

For external use only

When using this product

When using this product, avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor

if redness and irrigation develop and last

Keep out of reach of children

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

Directions

Apply onto wet hands. Lather and rinse thoroughly

Other information

Store at room temperature

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 EUCALYPTUS ANTIBACTERIAL HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77731-057
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: 77731-057-01	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)