KAI KLEAN- alcohol liquid

KAI KLEAN by

Drug Labeling and Warnings

KAI KLEAN by is a Otc medication manufactured, distributed, or labeled by Bender Consulting Ltd, BINH TAY LICO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

KAI KLEAN 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74918-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74918-002-27	2700 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020
2	NDC: 74918-002-20	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020
3	NDC: 74918-002-18	1800 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020
4	NDC: 74918-002-10	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/08/2020
5	NDC: 74918-002-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020
6	NDC: 74918-002-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020
7	NDC: 74918-002-00	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/08/2020

Labeler - Bender Consulting Ltd (036411509)

Registrant - Bender Consulting Ltd (036411509)

Establishment
Name	Address	ID/FEI	Business Operations
BINH TAY LICO		555362337	manufacture(74918-002) , pack(74918-002)