FDA.reportPublic FDA data

SMART SAN HAND SANITIZER FRAGRANCE-FREE

Manufacturer
Best Sanitizers, Inc.
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:44:01

Label at a glance#

ProductSMART SAN HAND SANITIZER FRAGRANCE-FREE
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information store in a cool, dry place below 104 o F (40 o C)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl alcohol 71.0%

OTC - PURPOSE SECTION

Purpose

Hand Sanitizer

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings

  • 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
  • for external use only

OTC - STOP USE SECTION

Stop use and ask a doctor ifirritation 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.

DOSAGE & ADMINISTRATION SECTION

Directions

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

STORAGE AND HANDLING SECTION

Other information

store in a cool, dry place below 104 oF (40 oC)

INACTIVE INGREDIENT SECTION

Inactive ingredents

Water, Isopropanol, glycerin, glycerol monolaurate

OTC - QUESTIONS SECTION

Questions?

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Smart

San

hand sanitizer spray

with natural emollients

to soften hands

kills 99.9999% of

26 tested pathogens

fragrance-free

Net Contents:

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041882ethanol 71 % Topical SprayPSN2
1041882ethanol 0.71 ML/ML Topical SpraySCD2
1041882ethanol 71 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59900-126-04SMART SAN HAND SANITIZER FRAGRANCE-FREE1000 mL in 1 BOTTLELIQUID10002
59900-126-07SMART SAN HAND SANITIZER FRAGRANCE-FREE500 mL in 1 BOTTLELIQUID5002
59900-126-10SMART SAN HAND SANITIZER FRAGRANCE-FREE59 mL in 1 BOTTLELIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59900-126SMART SAN HAND SANITIZER FRAGRANCE-FREE (ALCOHOL) LIQUID [BEST SANITIZERS, INC.]2Current NDC, Legacy NDC, 3 package rows20241218_bce412dc-21db-4c63-b4fc-33538cda7424.zip

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
59900-12659900-126-04, 59900-126-07, 59900-126-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL LAURATEY98611C087IACT
ALCOHOL3K9958V90MACTIB

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
SMART SAN HAND SANITIZER FRAGRANCE-FREEALCOHOLBest Sanitizers, Inc.bce412dc-21db-4c63-b4fc-33538cda74242024-12-05WarningsExact identifier
ndc (package): 59900-126-10
ndc (package): 59900-126-04
ndc (package): 59900-126-07
ndc (product): 59900-126
ndc11 (package): 59900012604
ndc11 (package): 59900012607
ndc11 (package): 59900012610
spl id: 288cba7a-1f75-6d80-e063-6394a90aca47
spl set id: bce412dc-21db-4c63-b4fc-33538cda7424

Reported adverse events (FAERS/openFDA)#

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