DR.BELLCA HAND SANITIZER GEL- hand sanitizer gel

Dr.Bellca Hand Sanitizer Gel by

Drug Labeling and Warnings

Dr.Bellca Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Oneskin Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

ACTIVE INGREDIENT

Ethyl Alcohol 70%

PURPOSE

Antimicrobial

INDICATIONS & USAGE

• Hand sanitizer to help reduce bacteria on the skin.

DOSAGE & ADMINISTRATION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Childern under 6 years of age should be supervised when using Dr.Bellca Hand Sanitizer.

STORAGE AND HANDLING

Store below 110oF (43oC).
May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT

Water, Glycerin, Carbomer, Tetrahydroxypropyl Ethylenediamine, Orange Oil, Peppermint Oil, Sodium Hyaluronate, Allantoin, Mugwort Extract, Green Tea Extract.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.BELLCA HAND SANITIZER GEL 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70889-800
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER 940 (UNII: 4Q93RCW27E)
EDETOL (UNII: Q4R969U9FR)
ORANGE OIL (UNII: AKN3KSD11B)
PEPPERMINT OIL (UNII: AV092KU4JH)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALLANTOIN (UNII: 344S277G0Z)
ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70889-800-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/23/2020
2	NDC: 70889-800-02	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/23/2020
3	NDC: 70889-800-03	1 in 1 BOX	03/23/2020
3		50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/23/2020

Labeler - Oneskin Cosmetics Co., Ltd. (689846630)

Registrant - Oneskin Cosmetics Co., Ltd. (689846630)

Establishment
Name	Address	ID/FEI	Business Operations
Oneskin Cosmetics Co., Ltd.		689846630	manufacture(70889-800)