Kong HandiPOD

Manufacturer
HANDIPOD LIMITED
Effective date
2023-11-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:22:09

Label at a glance#

ProductKong HandiPOD
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce germs on the skin.

Dosage and administration

• Put enough product in your palm to cover hands and rub hands together briskly until dry, ensuring contact with finger nails and in between fingers. Do not use on damaged, sensitive or irritated skin. • Children under 6 years of age should be supervised when using this hand sanitizer.

Label contents#

Full prescribing information#

Active Ingredinet

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70.0% v/v (70.0g/per 100g)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce germs on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

do not use

OTC - DO NOT USE SECTION

in or near the eyes. In case of contact, remove contact lenses if present, rinse thoroughly with water for several minutes. If eye irritation persists: Get medical attention - show this packaging or gel container.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Put enough product in your palm to cover hands and rub hands together briskly until dry, ensuring contact with finger nails and in between fingers. Do not use on damaged, sensitive or irritated skin. • Children under 6 years of age should be supervised when using this hand sanitizer.

Other Information

SPL UNCLASSIFIED SECTION

• Store below 110⁰F (43⁰C). Store in a well ventilated place. • May discolor certain fabrics or surfaces • Keep out of reach of children. If swallowed seek medical advice immediately and show this packaging or gel container. • Microbiological Testing: Bactericidal according to: BS EN1500.


Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat, Aqua, Carbomer, Glycerin, Aminomethylpropanol, parfum CI 17200, 42090.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71427-21371427-213-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
0fc686ed-0167-e6b9-e063-6294a90a55d6352993f4-f076-476e-b2e5-b9ff0af5eeec2024-01-25WarningsExact identifier
spl set id: 352993f4-f076-476e-b2e5-b9ff0af5eeec

Reported adverse events (FAERS/openFDA)#

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