FDA.reportPublic FDA data

Benza Clean hand sanitizer

Manufacturer
BIOSYN INC
Effective date
2020-09-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:00

Label at a glance#

ProductBenza Clean hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. As a wound antiseptic to help prevent bacterial contamination in cuts, burns, scrapes, lacerations and skin infections.

Dosage and administration

Pump onto hands as needed. Rub briskly until dry. Apply to wounds 3 times per day after cleaning. Allow to dry. May be bandaged once dry.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% 

Purpose

OTC - PURPOSE SECTION

Antimicrobial and First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin. As a wound antiseptic to help prevent bacterial contamination in cuts, burns, scrapes, lacerations and skin infections.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. Incase of eye contact, flush eyes with water.
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

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 onto hands as needed. Rub briskly until dry.
  • Apply to wounds 3 times per day after cleaning. Allow to dry. May be bandaged once dry.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Bicarbonate, Colalipid C, Hydroxyethyl Cellulose, Green Tea Leaf Extract.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79832-001-012022-01-28C16284748780-1d6a99b39-b0ef-a426-e053-dadaa90af4c21509ef50-c1d6-4161-8674-e644a8811684
79832-001-022022-01-28C16284748780-1d6a99b39-b0ef-a426-e053-dadaa90af4c21509ef50-c1d6-4161-8674-e644a8811684

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79832-001BENZA CLEAN HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [BIOSYN INC]1Legacy NDC20201006_1509ef50-c1d6-4161-8674-e644a8811684.zip

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
79832-00179832-001-01, 79832-001-02

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOIACT
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
GREEN TEA LEAFW2ZU1RY8B0IACT

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
dbdb0bef-128a-45c2-a443-d64b62627d361509ef50-c1d6-4161-8674-e644a88116842020-09-26WarningsExact identifier
spl id: dbdb0bef-128a-45c2-a443-d64b62627d36
spl set id: 1509ef50-c1d6-4161-8674-e644a8811684

Reported adverse events (FAERS/openFDA)#

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