Nineteen Certified Hand Sanitizer

Manufacturer
Lopez-Scripa Industries LLC
Effective date
2020-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:36

Label at a glance#

ProductNineteen Certified Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand anitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Do not use on children less than 2 months of age. Do not use on open wounds.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 80%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

17-18% Sterilized Water, 1.5 % Glycerin 0.2% Hydrogen Peroxide 34%, Less than 0.01% Bittering Agent

USES

INDICATIONS & USAGE SECTION

Hand anitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Do not use on children less than 2 months of age. Do not use on open wounds.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY - HANDS

FLAMMABLE - KEEP AWAY FROM HEAT AND FLAME

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE AND ASK A DOCTOR

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF THE REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center right away.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C). May discolor some fabrics. Harmful to wood finishes and plastics.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79526-000-012022-01-28C16284748780-1d6a99b39-e00f-a426-e053-dadaa90af4c2Nineteen Certified Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79526-000-01Nineteen Certified Hand Sanitizer3785.41 mL in 1 BOTTLELIQUID3785.411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79526-000NINETEEN CERTIFIED HAND SANITIZER (ALCOHOL) LIQUID [LOPEZ-SCRIPA INDUSTRIES LLC]1Legacy NDC, 1 package rows20200813_acb1ead8-765f-2717-e053-2a95a90a4ec5.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79526-00079526-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
acb076ea-8a83-f89b-e053-2a95a90ab517acb1ead8-765f-2717-e053-2a95a90a4ec52020-08-12WarningsExact identifier
spl id: acb076ea-8a83-f89b-e053-2a95a90ab517
spl set id: acb1ead8-765f-2717-e053-2a95a90a4ec5

Reported adverse events (FAERS/openFDA)#

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