FDA.reportPublic FDA data

Seal-D All Day Protection Hand Sanitizer

Manufacturer
Advanced Nanocoatings, Inc
Effective date
2020-10-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:13:30

Label at a glance#

ProductSeal-D All Day Protection Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Hand Sanitizer to help decrease 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 decrease bacteria 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 if

OTC - STOP USE SECTION

  • 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.

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

LabelLabel

Package Labeling:200ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

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
80742-00080742-000-00, 80742-000-01

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
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDEGLJ50K866TIACT

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
ef1b8b74-8159-8f4f-e053-2a95a90a79b2b0b55492-b522-b4f1-e053-2995a90ac1562022-12-05WarningsExact identifier
spl set id: b0b55492-b522-b4f1-e053-2995a90ac156

Reported adverse events (FAERS/openFDA)#

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