ANTIBACTERIAL HAND GEL Tootsie Roll Vanilla

Label at a glance#

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Decrease bacteria on hands

Warnings

WARNINGS SECTION

External Use Only. DO NOT EAT.

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.

WARNINGS SECTION

Flammable: Keep away from flame or high heat

Directions

DOSAGE & ADMINISTRATION SECTION

Rub hands thoroughly with product and allow to dry.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Blue NO.1

Stop and Ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develop.

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 71246-5029

NDC: 71246-5029-1 40 mL in a POUCH

HAND SANITIZER VANILLA (ALCOHOL) GEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

• Hand Sanitizer Vanilla
• Alcohol
• PROPYLENE GLYCOL
• WATER
• GLYCERIN
• CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)
• TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE
• VANILLA
• FD&C BLUE NO. 1

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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.

Reported adverse events (FAERS/openFDA)#

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