PERSANI HAND SANITIZER- alcohol liquid

Persani Hand Sanitizer by

Drug Labeling and Warnings

Persani Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Wisconsin Pharmacal Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

• Active ingredient: Purpose
• Alcohol 80% v/v: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Uses

■ Hand sanitizer to help reduce bacteria that can potentially 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

■ on children less than 2 months of age ■ on open skin wounds

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

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. 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.
■ Allow to dry without wiping.

Other information

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

Inactive ingredients

Glycerin, Hydrogen peroxide, Purified water USP

Questions or comments?

1-800-635-3696

Package Label - Principal Display Panel

PERSÀNI

Alcohol Antiseptic 80%

TOPICAL SOLUTION

Hand Sanitizer

Non-Sterile Solution

NET WT 4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

PERSANI HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-7122
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-7122-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

Labeler - Wisconsin Pharmacal Company (800873986)

Establishment
Name	Address	ID/FEI	Business Operations
Wisconsin Pharmacal Company		800873986	manufacture(68093-7122) , pack(68093-7122) , label(68093-7122)