Hand Sanitizer

Manufacturer
Lil' Drug Store Products, Inc
Effective date
2017-12-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:06:39

Label at a glance#

ProductHand Sanitizer Lil Drug Store Products, Inc.
Active ingredientAlcohol
Label structure10 sections

Dosage and administration

Wet hands with product and rub briskly until dry.

Storage and handling

Do not store above 100°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops or persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands with product and rub briskly until dry.

Other Information

STORAGE AND HANDLING SECTION

Do not store above 100°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Triethanolamine, Glycerin, Propylene Glycol, Carbomer, Fragrance, Isopropyl Myristate, Tocopheryl Acetate, Aloe Barbadensis Gel

SPL UNCLASSIFIED SECTION

Proudly distributed by Circle K Stores Inc.

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

K®

Instant
Hand Sanitizer
Moisturizing with
Vitamin E & Aloe

Kills 99.99% of
Harmful Germs

0.5 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 15 mL Bottle Label

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66715-576366715-5763-0
64893-030

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
19b525ab-e37c-41f0-b4fb-83b73554d55cadb7b8c0-44e7-4499-85d4-2d4e54f790622017-12-13WarningsExact identifier
spl id: 19b525ab-e37c-41f0-b4fb-83b73554d55c
spl set id: adb7b8c0-44e7-4499-85d4-2d4e54f79062

Reported adverse events (FAERS/openFDA)#

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