HANICO LAB HAND SANITIZER GEL- alcohol gel

Hanico LAB HAND SANITIZER gel by

Drug Labeling and Warnings

Hanico LAB HAND SANITIZER gel by is a Otc medication manufactured, distributed, or labeled by HLK Bio Co., Ltd., i Mine Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70%

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

Water, Carbomer, Triethanolamine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANICO LAB HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78552-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78552-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2020
2	NDC: 78552-001-02	100 mL in 1 TUBE; Type 0: Not a Combination Product	06/05/2020
3	NDC: 78552-001-03	200 mL in 1 TUBE; Type 0: Not a Combination Product	06/05/2020
4	NDC: 78552-001-04	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/05/2020
5	NDC: 78552-001-05	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/05/2020

Labeler - HLK Bio Co., Ltd. (695700923)

Registrant - HLK Bio Co., Ltd. (695700923)

Establishment
Name	Address	ID/FEI	Business Operations
i Mine Co.,Ltd.		557816813	manufacture(78552-001)