BONANGE HAND CLEANER- alcohol gel

BONANGE HAND CLEANER by

Drug Labeling and Warnings

BONANGE HAND CLEANER by is a Otc medication manufactured, distributed, or labeled by Mi-face Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT: ALCOHOL 70.0% w/w

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:

Water, Glycerin, Phenoxyethanol, Carbomer, Triethanolamine, Butylene Glycol, 1,2-Hexanediol, PEG-60 Hydrogenated Castor Oil, Lavandula Angustifolia (Lavender) Oil, Opuntia Ficus-Indica Extract, Bambusa Vulgaris Leaf/Stem Extract, Avena Sativa (Oat) Kernel Extract, Luffa Cylindrica Fruit Extract, Aloe Barbadensis Leaf Extract, Salvia Hispanica Seed Extract, Cocos Nucifera (Coconut) Fruit Extract, Butyrospermum Parkii (Shea) Butter Extract, Scutellaria Baicalensis Extract, Laminaria Japonica Extract, Ethylhexylglycerin

PURPOSE

PURPOSE: ANTISEPTIC

KEEP OUT OF REACH OF CHILDREN

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

Uses:

Uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Directions

Directions:

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

Other information
Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Package Label: BONANGE HAND CLEANER 300mL

Package Label: BONANGE HAND CLEANER 500mL

INGREDIENTS AND APPEARANCE

BONANGE HAND CLEANER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75005-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
Phenoxyethanol (UNII: HIE492ZZ3T)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
Trolamine (UNII: 9O3K93S3TK)
Butylene Glycol (UNII: 3XUS85K0RA)
1,2-Hexanediol (UNII: TR046Y3K1G)
PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG)
LAVENDER OIL (UNII: ZBP1YXW0H8)
OPUNTIA FICUS-INDICA WHOLE (UNII: 23Z87HTQ6P)
BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
OAT (UNII: Z6J799EAJK)
LUFFA AEGYPTIACA FRUIT (UNII: QKL9NEO1F9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHIA SEED (UNII: NU0OLX06F8)
COCONUT (UNII: 3RT3536DHY)
SHEA BUTTER (UNII: K49155WL9Y)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
LAMINARIA JAPONICA (UNII: WE98HW412B)
Ethylhexylglycerin (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75005-020-01	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020
2	NDC: 75005-020-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Mi-face Co., Ltd (694820628)

Registrant - Mi-face Co., Ltd (694820628)

Establishment
Name	Address	ID/FEI	Business Operations
Mi-face Co., Ltd		694820628	manufacture(75005-020)