GERM AWAY- anti-microbial wipe cloth

Germ Away by

Drug Labeling and Warnings

Germ Away by is a Otc medication manufactured, distributed, or labeled by Unico International Trading Corp., Dan Mor. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Keep out of the reach of children.

Keep out of reach of children, except with adult supervision.

Warnings

For external use only. Do not use in the eyes.

Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours.

If swallowed, seek medical attention or contact a Poison Control Center.

Use

For use: gently pull wipe from the dispenser feed at an angle and in a downward motion. wet hands or surface thoroughly with the product and let dry, discard wipe in trash.

Inactive Ingredients

Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Fragrance, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

Purpose

Anti-bacterial

To Dispense

To dispense: locate tier notch on top of refill pouch. Tear straight across to open. Pull first wipe from canister of roll through the pouch center opening. Thread white through dispenser nozzle. If available, adjust nozzle wipe tension on dispenser. Use only upward pole dispensers (floor stand or wall unit) so liquid does not drip out of pouch.

Directions

To dispense: locate tier notch on top of refill pouch. Tear straight across to open. Pull first wipe from canister of roll through the pouch center opening. Thread white through dispenser nozzle. If available, adjust nozzle wipe tension on dispenser. Use only upward pole dispensers (floor stand or wall unit) so liquid does not drip out of pouch.

Package Label

INGREDIENTS AND APPEARANCE

GERM AWAY 
anti-microbial wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74680-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.001

Inactive Ingredients
Ingredient Name	Strength
PANTHENOL (UNII: WV9CM0O67Z)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
CHAMOMILE (UNII: FGL3685T2X)
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74680-101-88	1200 in 1 PACKAGE; Type 0: Not a Combination Product	05/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/23/2020

Labeler - Unico International Trading Corp. (805757200)

Registrant - Dan Mor (514523067)

Establishment
Name	Address	ID/FEI	Business Operations
Dan Mor		514523067	manufacture(74680-101)