Hand Sanitizer Topical Solution

Manufacturer
Scientific Labs
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:41

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

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 products to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flamable. Keep away from heat or flame

Do not use:

OTC - DO NOT USE SECTION

• In children less than 2 months of age
• on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, riege 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 reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

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 products to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP, sodium polyacrylate, triethanolamine, Propylene glycol

Package Labeling:1LT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:5LT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79796-000-012022-01-28C16284748780-1d6a99b39-f8ec-a426-e053-dadaa90af4c2Hand Sanitizer Topical Solution
79796-000-022022-01-28C16284748780-1d6a99b39-f8ec-a426-e053-dadaa90af4c2Hand Sanitizer Topical Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79796-000-01Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
79796-000-02Hand Sanitizer5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79796-000HAND SANITIZER (ALCOHOL) GEL [SCIENTIFIC LABS]1Legacy NDC, 2 package rows20200804_abfe6688-f86b-ba8e-e053-2995a90a49a3.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79796-00079796-000-01, 79796-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
abfe6688-f86c-ba8e-e053-2995a90a49a3abfe6688-f86b-ba8e-e053-2995a90a49a32020-08-03WarningsExact identifier
spl id: abfe6688-f86c-ba8e-e053-2995a90a49a3
spl set id: abfe6688-f86b-ba8e-e053-2995a90a49a3

Reported adverse events (FAERS/openFDA)#

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