FDA.reportPublic FDA data

Skin Block Extra Strength Hand Sanitizer

Manufacturer
Charter Oak Development Corporation
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:21:18

Label at a glance#

ProductSkin Block Extra Strength Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand and skin anti-microbial to help decrease pathogens (bacteria & germs) 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. Repeat as necessary.

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 and skin anti-microbial to help decrease pathogens (bacteria & germs) on the skin. Recommended for repeated use

Warnings:

WARNINGS SECTION

Do not freeze  For external use only 

Do not use 

OTC - DO NOT USE SECTION

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 irritation 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. Repeat as necessary.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Polyaminopropyl biguanide, 1-Octadecanaminum NN dimethyl (3- trimethoxysily) propyl chloride, C12-15 Pareth 12, Caprylyl Glucoside, Sodium Benzoate, Glycerin, Aloe Barbadensis Leaf Juice Extract, Citric Acid

Package Labeling:50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:200ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80254-00080254-000-00, 80254-000-01, 80254-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
CAPRYLYL GLUCOSIDEV109WUT6RLIACT
SODIUM BENZOATEOJ245FE5EUIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
2cd80b76-788e-d75e-e063-6394a90af3b8ae7ef91c-261a-ca13-e053-2995a90a54a72025-01-29WarningsExact identifier
spl set id: ae7ef91c-261a-ca13-e053-2995a90a54a7

Reported adverse events (FAERS/openFDA)#

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