FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Gemini Industries Inc.
Effective date
2020-07-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:16

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 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 product to avoid swallowing.

Storage and handling

Store below 110*F (43*C) may dis color certain fabrics/surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Use as hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. 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

OTC - WHEN USING SECTION

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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 product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110*F (43*C) may dis color certain fabrics/surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, purified water USP, hydroxyethylcellulose

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3780 mL NDC: 79730-003-01 3780 ml label3780 ml label

18930 mL NDC: 79730-003-05 18930 ml label18930 ml label

208197648 mL NDC: 79730-003-55 20819764 ml label20819764 ml label

124918530 mL NDC: 79730-003-33 124918530 ml label124918530 ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79730-003-012022-01-28C16284748780-1d6a99b39-5e0f-a426-e053-dadaa90af4c2abaacdeb-2434-261a-e053-2995a90ae34e
79730-003-052022-01-28C16284748780-1d6a99b39-5e0f-a426-e053-dadaa90af4c2abaacdeb-2434-261a-e053-2995a90ae34e
79730-003-332022-01-28C16284748780-1d6a99b39-5e0f-a426-e053-dadaa90af4c2abaacdeb-2434-261a-e053-2995a90ae34e
79730-003-552022-01-28C16284748780-1d6a99b39-5e0f-a426-e053-dadaa90af4c2abaacdeb-2434-261a-e053-2995a90ae34e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79730-003-01Hand Sanitizer3780 mL in 1 JUGGEL37802
79730-003-05Hand Sanitizer18930 mL in 1 JUGGEL189302
79730-003-33Hand Sanitizer1249185300 mL in 1 TANKGEL12491853002
79730-003-55Hand Sanitizer208197648 mL in 1 DRUMGEL2081976482

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79730-003HAND SANITIZER (ALCOHOL) GEL [GEMINI INDUSTRIES INC.]2Legacy NDC, 4 package rows20200731_abaacdeb-2434-261a-e053-2995a90ae34e.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79730-00379730-003-01, 79730-003-05, 79730-003-55, 79730-003-33
74100-003

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)S38J6RZN16IACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
abaacdeb-2435-261a-e053-2995a90ae34eabaacdeb-2434-261a-e053-2995a90ae34e2020-07-30WarningsExact identifier
spl id: abaacdeb-2435-261a-e053-2995a90ae34e
spl set id: abaacdeb-2434-261a-e053-2995a90ae34e

Reported adverse events (FAERS/openFDA)#

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