LABCCIN SANITIZER GEL- alcohol gel

LABCCIN Sanitizer gel by

Drug Labeling and Warnings

LABCCIN Sanitizer gel by is a Otc medication manufactured, distributed, or labeled by Doori Cosmetics 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 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

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.

Direction

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

Inactive ingredients

Water, Butylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance, Glycerin, Paeonia Suffruticosa Root Extract, Camellia Sinensis Leaf Extract, Aloe Ferox Leaf Extract, CITRUS PARADISI (GRAPEFRUIT) FRUIT EXTRACT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LABCCIN SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50375-003
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)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
PAEONIA X SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE FEROX LEAF (UNII: 0D145J8EME)
GRAPEFRUIT (UNII: O82C39RR8C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50375-003-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/14/2020

Labeler - Doori Cosmetics Co., Ltd. (688227465)

Registrant - Doori Cosmetics Co., Ltd. (688227465)

Establishment
Name	Address	ID/FEI	Business Operations
Doori Cosmetics Co., Ltd.		688227465	manufacture(50375-003)