ZETTA HAND GEL- alcohol gel

Zetta Hand gel by

Drug Labeling and Warnings

Zetta Hand gel by is a Otc medication manufactured, distributed, or labeled by DBK Korea Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 62%

Purpose

Antimicrobial

Use

• Hand sanitizer to help reduce bacteria 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, rinse eyes thoroughly with water.

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 nough produt in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product

Other information

• Store below 110°F (43°C)
• May discolor certain fabrics or surfaces

Inactive ingredients

Carbomer, Triethanolamine, Glycerin, Butylene Glycol, Aloe Vera Gel, D-Panthenol, Tocopherol, Dipotassium Glycyrrhizate, Fragrance, Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZETTA HAND GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74170-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74170-001-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/03/2020

Labeler - DBK Korea Co., Ltd. (687907394)

Registrant - DBK Korea Co., Ltd. (687907394)

Establishment
Name	Address	ID/FEI	Business Operations
DBK Korea Co., Ltd.		687907394	manufacture(74170-001)