Sani eZe

Manufacturer
MENPER DISTRIBUTORS, INC.
Effective date
2021-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:43

Label at a glance#

ProductSani eZe
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                             Purpose

Isopropyl alcohol 72% v/v..................Antiseptic

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

WARNINGS SECTION

Warnings

For external use only. Flammable keep away from fire or flame.

Do not use

in the eyes. In case of contact, rinse eyes throughly with water.
in children less than two months of age
on open skin wounds
Stop use and ask a doctor if irritation and redness develop and 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 Posion Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

wet hands thoroughly with product
briskly rub hands together until dry
supervise children under 6 years of age when using this product to avoid swallowing.
Other information

store at 20° to 25°C (68° to 77°F) Avoid excessive heat and protect from freezing.
may discolor certain frabics

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aloe barbadensis leaf juice, aminomethyl propanol, carbomer, dl-alpha tocopherol acetate, fragrance, glycerin, isopropyl myristate, propylene glycol, water.

OTC - QUESTIONS SECTION

Questions or Comments?

Call 1-800-560-5223 M-F 9 AM TO 4 PM Eastern.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SANIEZEspraySANIEZEspray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53145-415-022023-07-28C16284748780-10191ceaa-71c4-198a-e063-dbdaa90aec3ec79a92da-a7d9-448d-ad67-3afcba11b5a1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53145-415-02Sani eZe60 mL in 1 BOTTLE, SPRAYSPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53145-415SANI EZE (ISOPROPYL ALCOHOL) SPRAY [MENPER DISTRIBUTORS, INC.]1Legacy NDC, 1 package rows20210416_c79a92da-a7d9-448d-ad67-3afcba11b5a1.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53145-41553145-415-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
92727fa3-68cc-4eac-a10c-ab9d9824e0b4c79a92da-a7d9-448d-ad67-3afcba11b5a12021-04-14WarningsExact identifier
spl id: 92727fa3-68cc-4eac-a10c-ab9d9824e0b4
spl set id: c79a92da-a7d9-448d-ad67-3afcba11b5a1

Reported adverse events (FAERS/openFDA)#

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