AL KOGEL HAND SANITIZER- alcohol gel

Al kogel Hand Sanitizer by

Drug Labeling and Warnings

Al kogel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Taizhou Yadai Daily-Use Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria on the skin

Recommended for repeated use

Warnings

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

When using this product, do not use in or near eyes

Stop use and ask a doctor if redness or irritation develop and last for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Directions

• Pump as needed into your palms and thoroughly spead on both hands. Rub into skin until dry.

Other Information

Store at room temperature no higher than 45 C (113 F) and under shade. Keep in closed containers and free from direct sunlight. 

Inactive Ingredients

Carbomer, Triethanolamine, Glycerin, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AL KOGEL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52989-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER 940 (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52989-006-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020
2	NDC: 52989-006-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020
3	NDC: 52989-006-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020
4	NDC: 52989-006-04	900 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020
5	NDC: 52989-006-05	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/03/2020

Labeler - Taizhou Yadai Daily-Use Co., Ltd. (529899639)

Establishment
Name	Address	ID/FEI	Business Operations
Taizhou Yadai Daily-Use Co., Ltd.		529899639	manufacture(52989-006)