CARDINAL HEALTH SANITIZER- alcohol aerosol, foam

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Available from:

Cardinal Health

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

- 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 Antimicrobial

Authorization status:

OTC monograph not final

Summary of Product characteristics

CARDINAL HEALTH SANITIZER - ALCOHOL AEROSOL, FOAM
CARDINAL HEALTH
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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Cardinal Health Aerosol Foam Sanitizer
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
Apply approx. 3g
Antimicrobial
Keep out of reach of children.
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 Ethyl alcohol 62.5%
INACTIVE INGREDIENTS Water (Aqua), Hydrofluorocarbon 152a, Isobutane,
Emulsifying Wax NF, Cetyl
Lactate, Steareth-2, Propane, Sodium Benzoate, Sodium Sesquicarbonate,
Fragrance (Parfum)
CARDINAL HEALTH SANITIZER
alcohol aerosol, foam
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 3517-523
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
0 .6 25 mg in 1 mg
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
Cardinal Health
WATER (UNII: 0 59 QF0 KO0 R)
1,1-DIFLUO RO ETHANE (UNII: 0 B1U8 K2ME0 )
STEARETH-2 (UNII: V56 DFE46 J5)
SO DIUM BENZO ATE (UNII: OJ245FE5EU)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:6 3517-523-15
12 in 1 CASE
1
4250 0 0 mg in 1 BOTTLE, SPRAY
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MA