EZ-448 ANTIBACTERIAL MOIST HAND- benzalkonium chloride swab

EZ-448 Antibacterial Moist Hand by

Drug Labeling and Warnings

EZ-448 Antibacterial Moist Hand by is a Otc medication manufactured, distributed, or labeled by Ez Products Of South Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.11%

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on the skin.

Warnings

For external use only.

Do not use 

in the eyes.

Do not flush.

Discontinue use if

irritation and redness develops. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

• Open label, remove one wipe, and unfold.
• Wet hands thoroughly with product and allow to dry without wiping. Do not flush.

Other information

• Store below 95°F (35°C).
• May discolor certain fabrics or surfaces.

Inactive ingredients

Water, Propylene Glycol, Phenoxythanol, Polyaminopropyl Biguanide, Lauryl Glucoside, Tetrasodium EDTA, 2-Broma-2-Nitropropane-1,3-Diol, Chamomilla Recutita Extract, Aloe Barbadensis Leaf Juice Powder, Citric Acid, Sodium Citrate

Package Labeling:

INGREDIENTS AND APPEARANCE

EZ-448 ANTIBACTERIAL MOIST HAND 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69446-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.11 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
EDETATE SODIUM (UNII: MP1J8420LU)
BRONOPOL (UNII: 6PU1E16C9W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69446-200-00	20 in 1 PACKAGE	12/18/2017
1		2.85 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/17/2017

Labeler - Ez Products Of South Florida, LLC (113456060)