Persani Instant Hand Sanitizer

Manufacturer: Wisconsin Pharmacal Company
Effective date: 2022-01-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:46:44

Label at a glance#

ProductPersani Instant Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

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

Drug Facts

SPL UNCLASSIFIED SECTION

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient	Purpose
Ethyl Alcohol 62%	Antimicrobial

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

OTHER SAFETY INFORMATION

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

OTC - WHEN USING SECTION

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

■ Avoid contact with broken skin.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ 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

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

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)

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	2
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	2
1020364	ethanol 62 % Topical Spray	SY	2
1020364	ethyl alcohol 62 % Topical Spray	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68093-7116-1	2024-01-30	C162847	48780-1	1030e365-1325-111a-e063-dadaa90a10e2	Persani Isntant Hand Sanitizer 6 OZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68093-7116-1	Persani Instant Hand Sanitizer	170.1 g in 1 CAN	SPRAY	170.1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68093-7116	PERSANI INSTANT HAND SANITIZER (ALCOHOL) SPRAY [WISCONSIN PHARMACAL COMPANY]	2	Legacy NDC, 1 package rows	20220114_a363bffb-739c-3115-e053-2995a90a27b3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

Persani Instant Hand Sanitizer
ALCOHOL
ALOE VERA LEAF
PEG/PPG-18/18 DIMETHICONE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
ALPHA-TOCOPHEROL ACETATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68093-7116	68093-7116-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
PEG/PPG-18/18 DIMETHICONE	9H0AO7T794	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d57c22e2-5099-64ea-e053-2a95a90a4004			a363bffb-739c-3115-e053-2995a90a27b3	2022-01-13	Warnings	Exact identifier spl id: d57c22e2-5099-64ea-e053-2a95a90a4004 spl set id: a363bffb-739c-3115-e053-2995a90a27b3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.