ALPHA E3 PRO Hand Sanitizer Spray 69335-005

Manufacturer
Alpha Chemical Services, Inc. | Best Sanitizers, Inc
Effective date
2025-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:10:55

Label at a glance#

ProductAlpha E3 PRO Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

sanitizes hands to help reduce bacteria that potentially can cause disease helps to prevent cross-contamination recommended for repeated use helps prevent drying of skin

Dosage and administration

wet hands thoroughly with spray, covering entire surface of hands, especially the fingernails and cuticles rub hands together until dry

Storage and handling

store in a cool, dry place below 104° F (40° C)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71.0%

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • sanitizes hands to help reduce bacteria that potentially can cause disease
  • helps to prevent cross-contamination
  • recommended for repeated use
  • helps prevent drying of skin

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product

  • do not use in or near eyes
  • use in a well-ventilated area

OTC - STOP USE SECTION

Stop use and consult a doctor if

irritation or redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, seek medical attention or contact Poison Control center immediately.

Directions

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 (40° C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, isopropanol, glycerin, glycerol monolaurate

Questions?

OTC - QUESTIONS SECTION

Contact at (800) 464-9872

Mon-Fri 9 am - 4pm PST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALPHA

E3 PRO

HAND SANITIZER SPRAY

FOR FOOD INDUSTRY PROFESSIONALS

Kills 99.9999% of 26 Tested Pathogens

Enhanced With Moisturizers

Koser and Pareve Certified

KC

PAREVE

NSF

Nonfood Compunds

Program Listed (E3)

Registration #168868

Net Contents: 1000mL (33.81 fl oz)

container label_02container label_02

container label_01container label_01

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69335-005-01Alpha E3 PRO Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICSPRAY37851
69335-005-02Alpha E3 PRO Hand Sanitizer1000 mL in 1 CARTRIDGESPRAY10001

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69335-00569335-005-01, 69335-005-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Alpha E3 PRO Hand SanitizerALCOHOLAlpha Chemical Services, Inc.3ca728d4-5482-046f-e063-6394a90a42802025-08-18WarningsExact identifier
ndc (package): 69335-005-02
ndc (package): 69335-005-01
ndc (product): 69335-005
ndc11 (package): 69335000501
ndc11 (package): 69335000502
spl id: 3ca728d4-5483-046f-e063-6394a90a4280
spl set id: 3ca728d4-5482-046f-e063-6394a90a4280

Reported adverse events (FAERS/openFDA)#

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