73582-0003_Bonblissity Antibacterial Foaming Hand Soap

Bonblissity Antibacterial Foaming Hand by

Drug Labeling and Warnings

Bonblissity Antibacterial Foaming Hand by is a Otc medication manufactured, distributed, or labeled by BONBLISS BEAUTY, INC., BEAUTY SKIN.CO.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BONBLISSITY ANTIBACTERIAL FOAMING HAND- benzalkonium chloride soap 
BONBLISS BEAUTY, INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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73582-0003_Bonblissity Antibacterial Foaming Hand Soap

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use

• For handwashing to decrease bacteria on the skin

Warnings

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush wwith water.

Stop use and ask a doctor if irritation develops and persists for more than 72 hours.

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

Directions

Dispense onto hands. Wet as needed

Rub and lather vigorously for at least 20 seconds.

Rinse and dry thoroughly.

Inactive ingredients

Water, Glycerin, Lauric Acid, Myristic Acid, Disodium Laureth Sulfosuccinate, Potassium Hydroxide, 1,2-Hexanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Citric Acid, Lavandula Angustifolia (Lavender) Extract, Aloe Barbadensis Leaf Extract, Beta-Glucan, Sodium Hyaluronate , Hydroxypropyltrimonium Hyaluronate, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, Ethylhexylglycerin, Sodium Benzoate, Disodium EDTA, Fragrance

BONBLISSITY ANTIBACTERIAL FOAMING HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73582-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.001 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURIC ACID (UNII: 1160N9NU9U)
MYRISTIC ACID (UNII: 0I3V7S25AW)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
JOJOBA OIL (UNII: 724GKU717M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
HYALURONIC ACID (UNII: S270N0TRQY)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73582-0003-1	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/14/2020	12/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/14/2020	12/28/2021

Labeler - BONBLISS BEAUTY, INC. (055735749)

Registrant - BONBLISS BEAUTY, INC. (055735749)

Establishment
Name	Address	ID/FEI	Business Operations
BEAUTY SKIN.CO.,Ltd.		688530942	manufacture(73582-0003)

Revised: 12/2021

Document Id: d456390a-bafb-8ba9-e053-2995a90a61d2

34390-5

Set id: 168fe1af-f238-4186-be46-2100a3925279

Version: 3

Effective Time: 20211229