FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
SNYDER MANUFACTURING CORP
Effective date
2021-10-24
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:30:51

Label at a glance#

ProductHAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE 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#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE  0.1%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

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.

USES

INDICATIONS & USAGE SECTION

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE 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.

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

WATER, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERETH-2 COCOATE, BEHENTRIMONIUM CHLORIDE, DIHYDROXYETHYL COCAMINE OXIDE, FRAGRANCE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL (Front)_GSEP_Hand Sanitizer_BKC 01pct01b LBL (Front)_GSEP_Hand Sanitizer_BKC 01pct

01b LBL (DF Box)_GSEP_Hand Sanitizer_BKC 01pct01b LBL (DF Box)_GSEP_Hand Sanitizer_BKC 01pct

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73038-10373038-103-11, 73038-103-12, 73038-103-13, 73038-103-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
cf202472-00df-a5c6-e053-2a95a90adfdc10635562-efe6-4e7a-a866-b1b3328ad1d82021-10-24WarningsExact identifier
spl id: cf202472-00df-a5c6-e053-2a95a90adfdc
spl set id: 10635562-efe6-4e7a-a866-b1b3328ad1d8

Reported adverse events (FAERS/openFDA)#

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