Foaming Alcohol Hand Sanitizer

Manufacturer
Betco Corp | Accra Pac, Inc. (DBA KIK-Indiana)
Effective date
2022-06-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:59:11

Label at a glance#

ProductFoaming Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To help decrease bacterial germs on the sk!in that could cause disease. For use when soap and water are not available. Recommended for repeated use.

Dosage and administration

• Shake well before using. • Spray product on hands, enough to cover all surfaces. Rub hands together until all surfaces are wet and fully covered. Continue rubbing untiil hands feel dry. Do not rinse or wipe off sanitizer. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INSTRUCTIONS FOR USE SECTION

  • To help decrease bacterial germs on the sk!in that could cause

disease. For use when soap and water are not available.

  • Recommended for repeated use.

Warnings

WARNINGS SECTION

Warnings
For external use only

• Do not puncture or incinerate.

• Do not store above 120°F (49°C).

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes.
• It splashed in eyes, rinse immediately and thoroughly with water.
• Do not use on chil'dren under 2 months of age.
• Do not use on open wounds.
• Discontinue use if irritation/redness occurs.

Stop use and ask a physician

OTC - STOP USE SECTION

Stop use and ask a physician if irritation occurs for more than 3 days, contact a physician.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• In case of ingestion, get medical help or contact a Poison Control Center immediately.

Directions

INDICATIONS & USAGE SECTION

• Shake well before using.

• Spray product on hands, enough to cover all surfaces. Rub hands together until all surfaces are wet and fully covered. Continue rubbing untiil hands feel dry. Do not rinse or wipe off sanitizer.

• Supervise children under 6 years of age when using this product to avoid swallowing.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

• Spray product on hands, enough to cover all surfaces. Rub hands together until all surfaces are wet and fully covered. Continue rubbing untiil hands feel dry. Do not rinse or wipe off sanitizer.

Other Information

OTHER SAFETY INFORMATION

• For best benefit, store and use are 55-85° F (13-29°C).

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Hydrofluorocarbon 152a, lsobutane, Emulsifying Wax., Cetyl Lactate, Steareth-2, Sodium Benzoate, Sodium Sesquicarbonate.
Fragrance

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

799E6799E6

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65601-30965601-309-01, 65601-309-02

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
275b707f-d824-f495-e063-6394a90ad72ca796ed97-a1a9-8529-e053-2a95a90a28ad2024-11-20WarningsExact identifier
spl set id: a796ed97-a1a9-8529-e053-2a95a90a28ad

Reported adverse events (FAERS/openFDA)#

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