FDA.reportPublic FDA data

G3Tech Hand Sanitizer

Manufacturer
Freshstart Holding Inc | G3 Blue Technology Pte Ltd
Effective date
2020-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:02

Label at a glance#

ProductG3Tech Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Squeeze a few drops onto palm. Rub onto entire area of hands, including backs, wirsts and between fingers until dry. No rinsing required.

Storage and handling

Store in a cool dry place Keep away from direct sunlight

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 10% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For External Use Only.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze a few drops onto palm.
  • Rub onto entire area of hands, including backs, wirsts and between fingers until dry.
  • No rinsing required.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place
  • Keep away from direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua,

Glycerin,

Anthemis Nobilis (Chamomile) Flower Water,

Acrylates/C 10-30 Alkyl Acrylate Crosspolymer,

Citric Acid,

Lavandula Angustifolia (Lavender) Oil,

Aloe Barbadensis Leaf Juice,

Hydroxypropyl Methylcellulose,

Curcumin,

Korean Pine Oil

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ml NDC: 79176-001-01 60ml label60ml label

500ml NDC: 79176-001-02

500 ml Label500 ml Label

1000ml NDC: 79176-001-03

1000ml label1000ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79176-001-012022-01-28C16284748780-1d6a99b39-df84-a426-e053-dadaa90af4c2ab83b445-0e2f-b985-e053-2995a90a0278
79176-001-022022-01-28C16284748780-1d6a99b39-df84-a426-e053-dadaa90af4c2ab83b445-0e2f-b985-e053-2995a90a0278
79176-001-032022-01-28C16284748780-1d6a99b39-df84-a426-e053-dadaa90af4c2ab83b445-0e2f-b985-e053-2995a90a0278

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79176-001-01G3Tech Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10001
79176-001-02G3Tech Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5001
79176-001-03G3Tech Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79176-001G3TECH HAND SANITIZER (HAND SANITIZER) GEL [FRESHSTART HOLDING INC]1Legacy NDC, 3 package rows20200807_ab83b445-0e2f-b985-e053-2995a90a0278.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79176-00179176-001-02, 79176-001-03, 79176-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAVENDER OILZBP1YXW0H8IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CURCUMINIT942ZTH98IACT
WATER059QF0KO0RIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
CHAMAEMELUM NOBILE FLOWER OILUB27587839IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
WHITE PINE OILHA5CX6676UIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ab83b445-0e31-b985-e053-2995a90a0278ab83b445-0e2f-b985-e053-2995a90a02782020-07-28WarningsExact identifier
spl id: ab83b445-0e31-b985-e053-2995a90a0278
spl set id: ab83b445-0e2f-b985-e053-2995a90a0278

Reported adverse events (FAERS/openFDA)#

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