FDA.reportPublic FDA data

Alpet E3 Plus Hand Sanitizer Spray

Manufacturer
Best Sanitizer, Inc.
Effective date
2010-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:59

Label at a glance#

ProductAlpet E3 Plus Hand Sanitizer Spray
Active ingredientEthanol
Label structure11 sections

Indications and uses

Sanitize hands to help reduce bacteria that potentially can cause disease Helps to prevent cross contamination Helps to prevent drying of the skin Recommended for repeated use

Storage and handling

Store in a cool dry place below 104° F

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 71%                

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • Sanitize hands to help reduce bacteria that potentially can cause disease
  • Helps to prevent cross contamination
  • Helps to prevent drying of the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • Do not use in or near eyes
  • Use in a well-ventilated area
  • Discontinue use if irritation and redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directons

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with spray, covering entire surface of hands, especially the fingernails and cuticles
  • Rub hands together until dry

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place below 104° F

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, isopropanol, glycerin, glycerol monolaurate

Questions?

OTC - QUESTIONS SECTION

Contact Best Sanitizers Mon-Fri 9am - 4p PST at 888-225-3267

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 59900-110-02

NDC: 59900-110-03

NDC: 59900-110-04

NDC: 59900-110-05

NDC: 59900-110-06

NDC: 59900-110-07

NDC: 59900-110-08

Alpet E3 Plus Hand Sanitizer Spray

For Food Industry Professionals


Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041882ethanol 71 % Topical SprayPSN1
1041882ethanol 0.71 ML/ML Topical SpraySCD1
1041882ethanol 71 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59900-110-022020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-032020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-042020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-052020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-062020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-072020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts
59900-110-082020-01-31C16284748780-19d75b9d0-5d49-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59900-110-02Alpet E3 Plus Hand Sanitizer Spray3785 mL in 1 BOTTLE, PLASTICLIQUID37851
59900-110-03Alpet E3 Plus Hand Sanitizer Spray189250 mL in 1 DRUMLIQUID1892501
59900-110-04Alpet E3 Plus Hand Sanitizer Spray500 mL in 1 BOTTLE, PLASTICLIQUID5001
59900-110-05Alpet E3 Plus Hand Sanitizer Spray1000 mL in 1 BOTTLE, PLASTICLIQUID10001
59900-110-06Alpet E3 Plus Hand Sanitizer Spray118 mL in 1 BOTTLE, PLASTICLIQUID1181
59900-110-07Alpet E3 Plus Hand Sanitizer Spray59 mL in 1 BOTTLE, PLASTICLIQUID591
59900-110-08Alpet E3 Plus Hand Sanitizer Spray1000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59900-110ALPET E3 PLUS HAND SANITIZER SPRAY (ETHANOL) LIQUID [BEST SANITIZER, INC.]1Legacy NDC, 7 package rows20100327_39ee1bb0-4c1b-4efd-b8ea-cc1070acc714.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EthanolACTIVE INGREDIENT3K9958V90M1
EthanolACTIVE MOIETY3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59900-11059900-110-02, 59900-110-03, 59900-110-04, 59900-110-05, 59900-110-06, 59900-110-07, 59900-110-08

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Ethanol3K9958V90MACTIB

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
7d4b3f7f-716f-4e42-9630-ecde825b3d5339ee1bb0-4c1b-4efd-b8ea-cc1070acc7142010-03-05WarningsExact identifier
spl id: 7d4b3f7f-716f-4e42-9630-ecde825b3d53
spl set id: 39ee1bb0-4c1b-4efd-b8ea-cc1070acc714

Reported adverse events (FAERS/openFDA)#

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