FDA.reportPublic FDA data

Smart San Hand Sanitizer Spray

Manufacturer
Best Sanitizers, Inc
Effective date
2010-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:00

Label at a glance#

ProductSmart San Hand Sanitizer Spray
Active ingredientEthanol
Label structure11 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

Store in a cool dry place below 104° F

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 71.0%

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

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

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.
  • For external use only
  • Discontinue use if irritation and redness develop If condition persists for more that 72 hours, consult a doctor.

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 center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with spray, covering entire surface of hands, especially the fingertips  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, fragrance, glycerin, glycerol monolaurate

Questions?

OTC - QUESTIONS SECTION

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

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 59900-111-02

NDC 59900-111-03

NDC 59900-111-04

NDC 59900-111-05

NDC 59900-111-06

Smart San™ Hand Sanitizer Spray


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
59900-111-022020-01-31C16284748780-19d75b9d0-00f7-f424-e053-dadaa90a57ceDrug Facts
59900-111-032020-01-31C16284748780-19d75b9d0-00f7-f424-e053-dadaa90a57ceDrug Facts
59900-111-042020-01-31C16284748780-19d75b9d0-00f7-f424-e053-dadaa90a57ceDrug Facts
59900-111-052020-01-31C16284748780-19d75b9d0-00f7-f424-e053-dadaa90a57ceDrug Facts
59900-111-062020-01-31C16284748780-19d75b9d0-00f7-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59900-111-02Smart San Hand Sanitizer Spray3785 mL in 1 BOTTLE, PLASTICLIQUID37851
59900-111-03Smart San Hand Sanitizer Spray189250 mL in 1 DRUMLIQUID1892501
59900-111-04Smart San Hand Sanitizer Spray500 mL in 1 BOTTLE, PLASTICLIQUID5001
59900-111-05Smart San Hand Sanitizer Spray1000 mL in 1 BOTTLE, PLASTICLIQUID10001
59900-111-06Smart San Hand Sanitizer Spray59 mL in 1 BOTTLE, PLASTICLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59900-111SMART SAN HAND SANITIZER SPRAY (ETHANOL) LIQUID [BEST SANITIZERS, INC]1Legacy NDC, 5 package rows20100327_d2a7fa32-8bce-4e4e-a7d5-e9ed852b5b0d.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
59900-11159900-111-02, 59900-111-03, 59900-111-04, 59900-111-05, 59900-111-06

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 · 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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7c2c757b-1280-4f42-a2af-49794269ff18d2a7fa32-8bce-4e4e-a7d5-e9ed852b5b0d2010-03-05WarningsExact identifier
spl id: 7c2c757b-1280-4f42-a2af-49794269ff18
spl set id: d2a7fa32-8bce-4e4e-a7d5-e9ed852b5b0d

Reported adverse events (FAERS/openFDA)#

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