Antibacterial hand sanitizer

Manufacturer
National Design LLC.
Effective date
2020-09-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:30

Label at a glance#

ProductAntibacterial hand sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

For hand sanitizing

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing

Warnings

WARNINGS SECTION

For external use only hands.

Flammable. Keep away from heat or flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes.  In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Other information:

DOSAGE & ADMINISTRATION SECTION

store at 20°C (68° to 77° F). may discolor fabrics.

Ingreidients:

INACTIVE INGREDIENT SECTION

Glycerin, propylene glycol, triethanolamine, carbomer, fragrance, disodium edta, tocopheryl acetate, deionized water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottleLabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812262ethanol 68 % Topical SprayPSN1
1812262ethanol 0.68 ML/ML Topical SpraySCD1
1812262ethanol 68 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80575-000-012022-01-28C16284748780-1d6a99b39-47d6-a426-e053-dadaa90af4c2Antibacterial hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80575-000-01Antibacterial hand sanitizer10 mL in 1 BOTTLE, SPRAYSPRAY101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80575-000ANTIBACTERIAL HAND SANITIZER (ALCOHOL) SPRAY [NATIONAL DESIGN LLC.]1Legacy NDC, 1 package rows20200930_afebe3de-b2c7-8130-e053-2995a90a9842.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80575-00080575-000-01

Ingredients#

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

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

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
afebed16-7fb3-330c-e053-2a95a90a79deafebe3de-b2c7-8130-e053-2995a90a98422020-09-22WarningsExact identifier
spl id: afebed16-7fb3-330c-e053-2a95a90a79de
spl set id: afebe3de-b2c7-8130-e053-2995a90a9842

Reported adverse events (FAERS/openFDA)#

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