SANI-TIZE E INSTANT HAND SANITIZER GEL

Manufacturer
Streamline Supply, Inc.
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:13

Label at a glance#

ProductSANI-TIZE E INSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other Information: May discolor some fabrics. Harmful to wood finishes and plastics. Store between 15-30°C (59-86°F). Avoid freezing and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethyl Alcohol 80% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic.

INDICATIONS & USAGE SECTION

Indications: Helps reduce bacteria on skin. Recommended for repeated use.

WARNINGS SECTION

Warnings: For external use only. Flammable, keep away from fire. Do not store above 104° F. Do not use on damaged or broken skin. Keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping. Use under adult supervision for children under 6. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Glycerin, hydrogen peroxide, purified water USP, carbomer.

STORAGE AND HANDLING SECTION

Other Information: May discolor some fabrics. Harmful to wood finishes and plastics. Store between 15-30°C (59-86°F). Avoid freezing and excessive heat above 40°C (104°F).

OTC - QUESTIONS SECTION

Emergency Phone: 1.800.633.8253

SPL UNCLASSIFIED SECTION

KILLS 99% OF GERMS

ALCOHOL BASED

WITH SOOTHING CONDITIONER

LEAVES HANDS FEELING CLEAN & MOISTURIZED

DERMATOLOGY TESTED

SDS and General Information: 1-877-350-5426

Email: info@streamlinesupply.com

STREAMLINE SUPPLY INC.

WWW.STREAMLINESUPPLY.COM

877-350-5426 • 460 NORTH 1000 WEST, CENTERVILLE, UT 84014

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77092-08077092-080-16, 77092-080-28

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 · Source PDF

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
4814b7fe-2108-4bf4-81c7-ab8f05f077fe46cf92f5-03c7-4050-be64-87bba90273e72020-12-31WarningsExact identifier
spl set id: 46cf92f5-03c7-4050-be64-87bba90273e7

Reported adverse events (FAERS/openFDA)#

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