SAN-EZ- isopropyl alcohol antiseptic 75% topical solution solution

SAN-EZ by

Drug Labeling and Warnings

SAN-EZ by is a Otc medication manufactured, distributed, or labeled by Dental Technologies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria that potentially can cause disease.
• For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30ºC between 15-30ºC (59-86ºF)
• Avoid freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Questions or comments?

Call 1-800-835-0885

Principal display panel

SAN-EZ™

ISOPROPYL ALCOHOL

ANTISEPTIC 75%

TOPICAL SOLUTION

HAND SANITIZER

NON-STERILE SOLUTION

8 fl. oz. (236 mL)

Principal display panel

SAN-EZ™

ISOPROPYL ALCOHOL

ANTISEPTIC 75%

TOPICAL SOLUTION

HAND SANITIZER

NON-STERILE SOLUTION

1.9 fl. oz. (55.5 mL)

INGREDIENTS AND APPEARANCE

SAN-EZ 
isopropyl alcohol antiseptic 75% topical solution solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55346-3301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55346-3301-1	55.5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/25/2020
2	NDC: 55346-3301-2	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/25/2020

Labeler - Dental Technologies, Inc. (148312838)

Registrant - Dental Technologies, Inc. (148312838)

Establishment
Name	Address	ID/FEI	Business Operations
Dental Technologies, Inc.		148312838	manufacture(55346-3301) , pack(55346-3301) , label(55346-3301)