KONG HANDIPOD- alcohol gel 
HANDIPOD LIMITED

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Kong HandiPOD

Drug Facts

Active Ingredinet

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

Purpose

Antimicrobial

Uses

  • Hand sanitizer to help reduce germs on the skin.

Warnings

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

When using this product

do not use

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

irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

• 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

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

Package Labeling:

Label

KONG HANDIPOD 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71427-213
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71427-213-4545 mL in 1 BOTTLE; Type 0: Not a Combination Product05/09/201705/06/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/09/201705/06/2021
Labeler - HANDIPOD LIMITED (220732701)

Revised: 1/2024
Document Id: 0fc686ed-0167-e6b9-e063-6294a90a55d6
Set id: 352993f4-f076-476e-b2e5-b9ff0af5eeec
Version: 3
Effective Time: 20240125
 
HANDIPOD LIMITED