INSTANT HAND SANITIZER- ethyl alcohol gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by AOSS Medical Supply, Inc. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
Ethyl Alcohol 62%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Uses
To help reduce bacteria on the hands that can potentially cause disease.

WARNINGS

Warning
For External Use Only.
Flammable, Keep away from fire or flame.

WHEN USING

When using this product
Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.

ASK DOCTOR

Ask a doctor before use if you have
Deep wounds, animal bites or serious burns.

STOP USE

Stop use and ask a doctor if
significant irritation or sensitization occurs.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

DIRECTIONS:
Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
Deionized water, Aloe barbadenis, Leaf Juice, Glycerin,
Propylene glycol, Carbomer, Aminomethyl Propanol, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53152-1004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53152-1004-1	118 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/28/2012

Labeler - AOSS Medical Supply, Inc. (787524651)