PERSANI INSTANT HAND SANITIZER- alcohol liquid

Persani Instant Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Purpose

Hand sanitizer to help reduce germs on the on the skin that can potentially cause disease

Drug Facts

Active Ingredient

• Active ingredient: Purpose
• Ethyl Alcohol 62%: Antimicrobial

Use

Hand sanitizer to help reduce germs on the on the skin that can potentially cause disease. Recomended for repeated use.

Warnings

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

When using this product Keep out of eyes. In case of eye contact, flush eyes with water. Avoid contact with broken skin.

Stop use and ask a doctor if irritation or redness develops, or if condition persist for more than 72 hours.

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

Directions

• Wet hands throughly with product.
• Rub hands together for 15 seconds, pay attention between fingers, fingernails and cuticles.
• Allow to dry without wiping.

Inactive ingredients

Aloe Vera, FD&C Blue#1, FD&C Yellow #5, Fragrance, PEG/PPG18/18 Dimethicone, Tocopheryl Acetate, Water

Questions or comments?

1-800-635-3696

Package Label - Principal Display Panel

Kills 99.99% of Germs

PERSANI

Instant

Hand Sanitizer

Ethyl Alcohol 62%

with Moisturizing

Vitamin E & Aloe

SmartScent

Odor Elimination Technology

NET WT 4 FL OZ (118.3 mL)

INGREDIENTS AND APPEARANCE

PERSANI INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-7110
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-7110-1	118.3 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/15/2020

Labeler - Wisconsin Pharmacal Company (800873986)

Establishment
Name	Address	ID/FEI	Business Operations
Wisconsin Pharmacal Company		800873986	manufacture(68093-7110) , pack(68093-7110) , label(68093-7110)