FDA.reportPublic FDA data

BioProtect Alcohol Free Hand Sanitizer

Manufacturer
Global BioProtect, LLC | Filltech USA, LLC
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:33:47

Label at a glance#

ProductBioProtect Alcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand Sanitizer to help derease bacteria on the skin - Recommended for repeated use.

Dosage and administration

Apply a small amount into palms and spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help derease bacteria on the skin - Recommended for repeated use.

Warnings:

WARNINGS SECTION

Do not freeze.

For external use only.

Do not use in ears or mouth.

When using this product,

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritaton develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should be supervised when using this product.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply a small amount into palms and spread on both hands. Rub into skin until dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Polyaminopropyl biguanide, 1-Octadecanaminum NN dimethyl(3-trime-thoxysilyl) propyl chloride, C12-15 Pareth 12, Caprylyl Glucoside, Sodium Benzoate, Aloe Barbadensis Leaf Juice Extract, Cironellol, Citric Acid, FD&A Blue No.1

Package Labling: 1890ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1

Package Labeling: 1890ml (Tilt & Pour)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling : 1000L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79141-00079141-000-01, 79141-000-02, 79141-000-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
C12-15 PARETH-12131316X18LIACT
CAPRYLYL GLUCOSIDEV109WUT6RLIACT
SODIUM BENZOATEOJ245FE5EUIACT
ALOE VERA LEAFZY81Z83H0XIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
cdc4c165-7315-951e-e053-2995a90a7f894807a276-aea3-4de8-ac49-9a9fc7f7b7bb2021-10-07WarningsExact identifier
spl id: cdc4c165-7315-951e-e053-2995a90a7f89
spl set id: 4807a276-aea3-4de8-ac49-9a9fc7f7b7bb

Reported adverse events (FAERS/openFDA)#

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