8.75OZ ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE- benzalkonium chloride gel

8.75oz ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE by

Drug Labeling and Warnings

8.75oz ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE by is a Otc medication manufactured, distributed, or labeled by Hero Brands, Inc., Zorin Pharmaceutical Technology (Hangzhou) Co Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.13% , Antibacterial

Purpose

Antibacterial, Hand SOAP

Use

For handwashing to decrease bacteria on skin.

Warnings

For external use only. Keep away from fire or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes. If contact with eyes occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash develops.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Wet hands
• Apply foaming soap to hands and work into rich lather
• Rinse hands thoroughly

Inactive ingredients

Disodium Cocoamphodiacetate,Water,Glycerin,Citric Acid, EDTA-2Na,CAB-35,Fragrance

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

8.75OZ ANTIBACTERIAL FOAM HANDSOAP - OCEAN BREEZE 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90114-253
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.013 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SHEA BUTTER (UNII: K49155WL9Y)
EDETIC ACID (UNII: 9G34HU7RV0)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90114-253-01	259 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/05/2020

Labeler - Hero Brands, Inc. (117527162)

Registrant - Hero Brands, Inc. (117527162)

Establishment
Name	Address	ID/FEI	Business Operations
Zorin Pharmaceutical Technology (Hangzhou) Co Ltd.		554529819	manufacture(90114-253)