Gator Byte

Manufacturer
Reliant Technologies
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:37

Label at a glance#

ProductGator Byte
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Directions : Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Under DirectionsUnder Directions

Warnings

WARNINGS SECTION

Warnings Section WarningWarning

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients section Inactive IngredientsInactive Ingredients

Usage and Indications

INDICATIONS & USAGE SECTION

Usage and Indications section Usage sectionUsage section

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children section Keep Out of Reach of ChildrenKeep Out of Reach of Children

Purpose Section

OTC - PURPOSE SECTION

Under purpose next to active ingredients PurposePurpose

Packaging Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785 mL (1 gallon) NDC: 78094-3740-1 3785 mL label3785 mL label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78094-001-012022-01-28C16284748780-1d6a99b39-8d7e-a426-e053-dadaa90af4c2Non-Alcohol Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78094-001-01Gator Byte100 g in 1 BOTTLELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78094-001GATOR BYTE (NON-ALCOHOL HAND SANITIZER) LIQUID [RELIANT TECHNOLOGIES]1Legacy NDC, 1 package rows20200602_a5f177a4-a68b-a880-e053-2a95a90a055b.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78094-00178094-001-01

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

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
a5f177a4-a68c-a880-e053-2a95a90a055ba5f177a4-a68b-a880-e053-2a95a90a055b2020-05-18WarningsExact identifier
spl id: a5f177a4-a68c-a880-e053-2a95a90a055b
spl set id: a5f177a4-a68b-a880-e053-2a95a90a055b

Reported adverse events (FAERS/openFDA)#

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