Hand Sanitizer

Manufacturer
General Organics Inc.
Effective date
2024-05-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:12:58

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

for hand-washing to decrease bacteria on the skin, only when water is not available

Dosage and administration

wet hand thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

  • Flammable, keep away from fire and flames
  • For external use ony

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hand thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, triethanolamine, carbopol, tween 20, glycerin, aloe

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76924-000-002025-08-26C16284748780-11030e364-faad-111a-e063-dadaa90a10e2Hand Sanitizer
76924-000-002025-07-29C16284748780-11030e364-faad-111a-e063-dadaa90a10e2Hand Sanitizer
76924-000-002024-05-24C16284748780-11030e364-faad-111a-e063-dadaa90a10e2Hand Sanitizer
76924-000-002024-01-30C16284748780-11030e364-faad-111a-e063-dadaa90a10e2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76924-000-00Hand Sanitizer236 mL in 1 BOTTLEGEL2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76924-000HAND SANITIZER (ALCOHOL) GEL [GENERAL ORGANICS INC.]3Legacy NDC, 1 package rows20240525_f34e6823-1ef0-49ff-9379-8c818d6d57d6.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76924-00076924-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
18ee9d95-8417-d31f-e063-6294a90a592cf34e6823-1ef0-49ff-9379-8c818d6d57d62024-05-20WarningsExact identifier
spl id: 18ee9d95-8417-d31f-e063-6294a90a592c
spl set id: f34e6823-1ef0-49ff-9379-8c818d6d57d6

Reported adverse events (FAERS/openFDA)#

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