FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Ruggiero Innovations, LLC
Effective date
2020-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:59:21

Label at a glance#

ProductHand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 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 liquid into palm of hand • Rub thoroughly over all surfaces of both hands for 15 seconds • Rinse with potable water (Optional).

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 

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use or ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Pump a small amount of liquid into palm of hand • Rub thoroughly over all surfaces of both hands for 15 seconds • Rinse with potable water (Optional).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

Package Labeling: 59ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 591ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

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
72155-01072155-010-01, 72155-010-02

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
COCO GLUCOSIDEICS790225BIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
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
b7b291d4-4b35-5fda-e053-2995a90ad854fa34b43a-683e-4e08-ab5b-c0c5832278e12020-12-30WarningsExact identifier
spl id: b7b291d4-4b35-5fda-e053-2995a90ad854
spl set id: fa34b43a-683e-4e08-ab5b-c0c5832278e1

Reported adverse events (FAERS/openFDA)#

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