CARDINAL HEALTH SANITIZER- alcohol aerosol, foam

Cardinal Health Sanitizer by

Drug Labeling and Warnings

Cardinal Health Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cardinal Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

Cardinal Health Aerosol Foam Sanitizer

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

Apply approx. 3g

PURPOSE

Antimicrobial

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

Warnings Flammable.
Keep away from fire or flame.
For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Contents under pressure. Do not puncture or incinerate container. Do not store at temperature above 120°F (48°C).

ACTIVE INGREDIENT

Active ingredient Ethyl alcohol 62.5%

INACTIVE INGREDIENT

Inactive Ingredients Water (Aqua), Hydrofluorocarbon 152a, Isobutane, Emulsifying Wax NF, Cetyl Lactate, Steareth-2, Propane, Sodium Benzoate, Sodium Sesquicarbonate, Fragrance (Parfum)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CARDINAL HEALTH SANITIZER 
alcohol aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63517-523
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.625 mg  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
STEARETH-2 (UNII: V56DFE46J5)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63517-523-15	12 in 1 CASE
1		425000 mg in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/24/2011

Labeler - Cardinal Health (097537435)