FDA.reportPublic FDA data

Safe Hands Foaming Hand Sanitizer Alcohol Free

Manufacturer
Celeste Industries Corporation
Effective date
2017-06-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:27

Label at a glance#

ProductSafe Hands Foaming Hand Sanitizer Alcohol Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • For external use only.

OTC - WHEN USING SECTION

  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycereth-26, Triethylene Glycol, Cocoamidopropyl PG-Dimonium Chloride Phosphate, Aroma, Hydroxyethylcellulose, Triethanolamine, DMDM Hydantoin and Iodopropynyl Butylcarbamate.

PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FOAMING HAND SANITIZER
Alcohol free

Kills 99% of germs on contact

Safe
Hands®

Requires no water or
towels. Apply small
amount to hands
and rub until dry.

Caution: Use on hands only.
8 fl oz • 236ml e

PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71489-00271489-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
GLYCERETH-26NNE56F2N14IACT
TRIETHYLENE GLYCOL3P5SU53360IACT
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%)X70SE62ZARIACT
TROLAMINE9O3K93S3TKIACT
DMDM HYDANTOINBYR0546TOWIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT

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
ee7b6e46-5070-4b9d-aa21-6e8a084f113a4de93686-6a79-4f4b-9cd0-e345a73b256f2019-12-23WarningsExact identifier
spl set id: 4de93686-6a79-4f4b-9cd0-e345a73b256f

Reported adverse events (FAERS/openFDA)#

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