PERSANI INSTANT HAND SANITIZER- alcohol spray

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 skin that can potentially cause disease.

Drug Facts

Active Ingredient

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

Uses

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

Warnings

For external use only.

■ Flammable: Keep away from fire or flame. ■ Contents under pressure.
Do not puncture or incinerate. Do not store at temperatures above 120F°(48C°).

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 persists 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 thoroughly 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/PPG-18/18 Dimethicone, Tocopheryl Acetate, Water

Package Label - Principal Display Panel

Kills 99.99% of Germs

Persani

Instant

Hand Sanitizer

Ethyl Alcohol 62%

with Moisturizing

Vitamin E & Aloe

SmartScent

Odor Eliminination Technology

Safe for the entire family

CONTINUOUS SPRAY

AT ANY ANGLE

NET WT 6 OZ (170.1 g)

INGREDIENTS AND APPEARANCE

PERSANI INSTANT HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-7116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-7116-1	170.1 g in 1 CAN; 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(68093-7116) , pack(68093-7116) , label(68093-7116)