FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
SNYDER MANUFACTURING CORP
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:19:30

Label at a glance#

ProductANTIBACTERIAL HAND
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

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

Label contents#

Full prescribing information#

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

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Coco Betaine, Sodium Coco Sulfate, Phenoxyethanol, Natural Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_hand soap small label_8oz01b LBL_hand soap small label_8oz

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73038-10473038-104-11

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCO-BETAINE03DH2IZ3FYIACT
SODIUM COCO-SULFATE3599J29ANHIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
cf1e6563-a22c-e995-e053-2a95a90a48a9c1ff573e-56f4-4ad7-b994-94bbdf83acc82021-10-24WarningsExact identifier
spl set id: c1ff573e-56f4-4ad7-b994-94bbdf83acc8

Reported adverse events (FAERS/openFDA)#

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