FDA.reportPublic FDA data

G3Tech Hand Sanitizer

Manufacturer
Freshstart Holdings Inc.
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:29:41

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 0.1% 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
79176-001-102022-01-28C16284748780-1d6a99b39-c93d-a426-e053-dadaa90af4c2af8f4efc-b57c-b449-e053-2a95a90ad659
79176-001-202022-01-28C16284748780-1d6a99b39-c93d-a426-e053-dadaa90af4c2af8f4efc-b57c-b449-e053-2a95a90ad659
79176-001-302022-01-28C16284748780-1d6a99b39-c93d-a426-e053-dadaa90af4c2af8f4efc-b57c-b449-e053-2a95a90ad659

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79176-001-10G3Tech Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10004
79176-001-20G3Tech Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5004
79176-001-30G3Tech Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79176-001G3TECH HAND SANITIZER (HAND SANITIZER) GEL [FRESHSTART HOLDINGS INC.]4Legacy NDC, 3 package rows20200918_af8f4efc-b57c-b449-e053-2a95a90ad659.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
79176-00179176-001-20, 79176-001-30, 79176-001-10

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
WHITE PINE OILHA5CX6676UIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CHAMAEMELUM NOBILE FLOWER OILUB27587839IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT

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
af8f7d9c-0c9e-2b04-e053-2995a90a83a0af8f4efc-b57c-b449-e053-2a95a90ad6592020-09-17WarningsExact identifier
spl id: af8f7d9c-0c9e-2b04-e053-2995a90a83a0
spl set id: af8f4efc-b57c-b449-e053-2a95a90ad659

Reported adverse events (FAERS/openFDA)#

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