GSD Advanced Hand Sanitizer

Manufacturer
JoCo Sales & Marketing, Inc.
Effective date
2020-05-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:28:18

Label at a glance#

ProductGSD Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Put enough product in yor palm to cover hands and rub hands together briskly until dry Children under 6 years of age shoud be supervised when using GSD ADVANCED HAND SANITIZER

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial 

Use

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable, Keep away from fire or flame.

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughy with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in yor palm to cover hands and rub hands together briskly until dry
  • Children under 6 years of age shoud be supervised when using GSD ADVANCED HAND SANITIZER

Other information

SPL UNCLASSIFIED SECTION

  • Store beow 86°F (30°C)
  • May discolor certain fabrics or surfaces. Keep away from sunlight

Innactive ingredients

INACTIVE INGREDIENT SECTION

  • Aqua, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Vera Extract.

Package Labeling:100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

FDA-Initiated Inactive NDC Indexing#

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
77784-00077784-000-00, 77784-000-01

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
eb74d128-2cf0-f95a-e053-2995a90af08de5814ac2-8fc8-4fdc-9adf-411223a611372022-10-20WarningsExact identifier
spl set id: e5814ac2-8fc8-4fdc-9adf-411223a61137

Reported adverse events (FAERS/openFDA)#

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