SANI EZE- isopropyl alcohol gel

Sani eZe by

Drug Labeling and Warnings

Sani eZe by is a Otc medication manufactured, distributed, or labeled by MENPER DISTRIBUTORS, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                             Purpose

Isopropyl alcohol 72% v/v..................Antiseptic

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

WARNINGS

Warnings

For external use only. Flammable keep away from fire or flame.

Do not use

in the eyes. In case of contact, rinse eyes throughly with water.
in children less than two months of age
on open skin wounds
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

wet hands thoroughly with product
briskly rub hands together until dry
supervise children under 6 years of age when using this product to avoid swallowing.
Other information

store at 20° to 25°C (68° to 77°F) Avoid excessive heat and protect from freezing.
may discolor certain frabics

INACTIVE INGREDIENT

Inactive ingredients

Aloe barbadensis leaf juice, aminomethyl propanol, carbomer, dl-alpha tocopherol acetate, fragrance, glycerin, isopropyl myristate, propylene glycol, water.

QUESTIONS

Questions or Comments?

Call 1-800-560-5223 M-F 9 AM TO 4 PM Eastern.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANI EZE 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	72 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER 940 (UNII: 4Q93RCW27E)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-410-02	60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/29/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/29/2011

Labeler - MENPER DISTRIBUTORS, INC. (101947166)