HELLO BELLO- ethyl alcohol liquid

Hello Bello by

Drug Labeling and Warnings

Hello Bello by is a Otc medication manufactured, distributed, or labeled by Brands International Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 75%

PURPOSE

Purpose -Antiseptic Skin cleanser 

INDICATIONS & USAGE

Use

• Antiseptic Skin cleanser

WARNINGS

Warnings

Keep away from open flame & sources of heat.

For extenal use only.

KEEP OUT OF REACH OF CHILDREN

Keep out of children

If accidently swallowed, call a posion control center or get medical help right away.

USER SAFETY WARNINGS

Do not get into eyes

If contact occurs, rinse thoroughly with water

DOSAGE & ADMINISTRATION

• Children,adolescents and adults 2 years and over.
• for occasional and personal domestic use
• supervise children when they use this product.
• Place enough product on your plam to thoroughly cover your hands.
• rub thoroughly into hands for at least 30 seconds
• Allow to dry.

OTHER SAFETY INFORMATION

Other Information

• May discolor certain fabrics or surfaces
• do not store above 110 F ( 43 C)

INACTIVE INGREDIENT

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Proylene glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E) Actetate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HELLO BELLO 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-120-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/18/2020

Labeler - Brands International Corp (243748238)