FIJI PUNCH HAND SANITIZER- alcohol antiseptic liquid

Fiji Punch Hand Sanitizer by

Drug Labeling and Warnings

Fiji Punch Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kingkey MBC Life Technology Group Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 62% ------------------------------- Antibacterial

Users

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Purpose

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Warnings

Flammable. Keep away from fire or flame.

For external use only.

Do not use it

near eye area. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children.

Keep out of reach of children.

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

Directions

■ Apply into hand and thoroughly spreadon both hands, rub until dry.

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

Inactives ingredient

Water
GLYCERIN
ALCOHOL
Fragrance
CI 17200
CI 16035

Other information

■ Store between 15 - 30°C ( 59 - 86°F )

■ Avoid freezing and excessive heat above 40°C (104°F )

Questions or comments？

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIJI PUNCH HAND SANITIZER 
alcohol antiseptic liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73928-128
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CI 16035 (UNII: WZB9127XOA)
CI 17200 (UNII: 9DBA0SBB0L)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73928-128-01	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	02/01/2025

Labeler - Kingkey MBC Life Technology Group Co.,Ltd (545349263)

Registrant - Kingkey MBC Life Technology Group Co.,Ltd (545349263)

Establishment
Name	Address	ID/FEI	Business Operations
Kingkey MBC Life Technology Group Co.,Ltd		545349263	manufacture(73928-128)