TOTAL SOLUTIONS ALCOHOL-FREE HAND SANITIZING WIPES- benzalkonium cloth

Total Solutions Alcohol-Free Hand Sanitizing Wipes by

Drug Labeling and Warnings

Total Solutions Alcohol-Free Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Athea Laboratories, Inc., Athea Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.12%

PURPOSE

Antiseptic

INDICATIONS & USAGE

• For handwashing to decrease bacteria on the skin.
• After changing diapers.
• After assisting ill persons.
• Before contact with a person under medical care or treatment.
• Recommended for repeat use.

WARNINGS

For external use only.

DO NOT USE

Do not use in the eyes.

WHEN USING

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

ASK DOCTOR/PHARMACIST

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

• Wet hands thoroughly with product and allow to dry.
• Children under six years of age should be supervised when using this product.

OTHER SAFETY INFORMATION

• Store in a cool, dry place.

INACTIVE INGREDIENT

Water, Aloe Barbadensis Leaf Juice, Polysorbate 20, Glycerin, Potassium Sorbate, Fragrance, Citric Acid, Disodium EDTA, Tocopheryl Acetate (Vitamin E).

70 Count

1600 count

INGREDIENTS AND APPEARANCE

TOTAL SOLUTIONS ALCOHOL-FREE HAND SANITIZING WIPES 
benzalkonium cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62819-445
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.12 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62819-445-00	70 in 1 CANISTER	01/03/2011
1		3.5 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 62819-445-01	1600 in 1 BAG	01/29/2013
2		3.5 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/03/2011

Labeler - Athea Laboratories, Inc. (078281547)

Establishment
Name	Address	ID/FEI	Business Operations
Athea Laboratories, Inc		006117816	label(62819-445) , manufacture(62819-445)