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 structure8 sections

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 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

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

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 persist 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, Fragrance, PEG/PPG18/18 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

NET WT 4 FL OZ (118.3 mL)

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	2
247835	ethanol 0.62 ML/ML Topical Solution	SCD	2
247835	ethanol 62 % Topical Solution	SY	2
247835	ethyl alcohol 62 % Topical Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68093-7110-1	2024-01-30	C162847	48780-1	1030e365-5e2f-111a-e063-dadaa90a10e2	Persani Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68093-7110-1	Persani Instant Hand Sanitizer	118.3 mL in 1 BOTTLE, PUMP	LIQUID	118.3		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68093-7110	PERSANI INSTANT HAND SANITIZER (ALCOHOL) LIQUID [WISCONSIN PHARMACAL COMPANY]	2	Legacy NDC, 1 package rows	20220114_a35fb7f4-3d32-db58-e053-2995a90a1421.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
ALPHA-TOCOPHEROL ACETATE
ALOE VERA LEAF
WATER
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
PEG/PPG-18/18 DIMETHICONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68093-7110	68093-7110-1

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

Source Document#

Source XML

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
d57c225b-6bbd-0c8f-e053-2a95a90ab8b5			a35fb7f4-3d32-db58-e053-2995a90a1421	2022-01-13	Warnings	Exact identifier spl id: d57c225b-6bbd-0c8f-e053-2a95a90ab8b5 spl set id: a35fb7f4-3d32-db58-e053-2995a90a1421

Reported adverse events (FAERS/openFDA)#

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