Persani 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 Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

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

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-800-635-3696

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

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

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.
Recomended 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 temperature 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 throughly 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, Fragance, PEG/PPG-18/18 Dimethicone, Tocopheryl Acetate, Water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-635-3696

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 Elimination Technology

Safe for the entire family

CONTINUOUS SPRAY

AT ANY ANGLE

NET WT 4 OZ (113 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
68093-7114-1	2024-01-30	C162847	48780-1	1030e365-4f37-111a-e063-dadaa90a10e2	Persani Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68093-7114-1	Persani Hand Sanitizer	113 g in 1 CAN	SPRAY	113		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68093-7114	PERSANI HAND SANITIZER (ALCOHOL) SPRAY [WISCONSIN PHARMACAL COMPANY]	2	Legacy NDC, 1 package rows	20220114_a3625488-7f92-f808-e053-2a95a90a9a4b.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68093-7114	68093-7114-1

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
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
PEG/PPG-18/18 DIMETHICONE	9H0AO7T794	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT

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
d57c1f46-847d-402d-e053-2995a90a7d67			a3625488-7f92-f808-e053-2a95a90a9a4b	2022-01-13	Warnings	Exact identifier spl id: d57c1f46-847d-402d-e053-2995a90a7d67 spl set id: a3625488-7f92-f808-e053-2a95a90a9a4b

Reported adverse events (FAERS/openFDA)#

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