FDA.reportPublic FDA data

Smart San Alcohol-Free Hand Sanitizer Foam

Manufacturer
Best Sanitizers, Inc.
Effective date
2019-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:24:17

Label at a glance#

ProductSmart San Alcohol-Free Hand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
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

Benzalkonium Chloride 0.12% w/w

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • sanitize 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

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 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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • receive a small amount of foam into palm of hand
  • rub thoroughly over all surfaces of both hands
  • rub hands together until dry

STORAGE AND HANDLING SECTION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, cocamidopropyl betaine, glycerin, poloxamer 124, phenoxyethanol, benzyl alcohol, dehydroacetic acid, sodium hydroxide, citric acid

OTC - QUESTIONS SECTION

Questions?

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

versaclenz compatible

Smart San

alcohol-free

hand sanitizer

foam

with natural

emollients to

soften hands

kills 99.9%-99.999%

of tested pathogens

Net Contents:

container labelcontainer label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59900-11959900-119-05, 59900-119-08, 59900-119-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
POLOXAMER 1241S66E28KXAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZYL ALCOHOLLKG8494WBHIACT
DEHYDROACETIC ACID2KAG279R6RIACT
SODIUM HYDROXIDE55X04QC32IIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
0eae6b96-e497-98ef-e063-6294a90af515424020fa-31ea-4c70-8dd8-0345342cf0b02024-01-11WarningsExact identifier
spl set id: 424020fa-31ea-4c70-8dd8-0345342cf0b0

Reported adverse events (FAERS/openFDA)#

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