Pure Grass Hand Sanitizer

Label at a glance#

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Organic Ethyl Alcohol 60%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings:

WARNINGS SECTION

For external use only.
Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop and persist for more than 72 hours.

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 immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product. Briskly rub hands together until dry. Supervise children under 6 years in the use of this product.

Other information:

OTHER SAFETY INFORMATION

Store at room temperature. May discolor certain fabrics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Fragrance (Parfum), Glycereth-7 Triacetate, Carbomer, Aminomethyl Propanol.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Good Home Co.
Established 1995

PURE GRASS®
Hand Sanitizer

Made with Organic Alcohol

8 oz/237 ml

The Good Home Co., Inc., New York, NY 10272

Label

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

• Pure Grass Hand Sanitizer
• Ethyl Alcohol
• ALCOHOL
• WATER
• GLYCERETH-7 TRIACETATE
• CARBOXYPOLYMETHYLENE
• AMINOMETHYLPROPANOL

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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.