Drug Facts

COCOBATH WATERLESS- benzalkonium chloride shampoo
giod Co.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Benzalkonium Chloride 0.1%

Antibacterial

Provide sanitizing when soap and water not available
Kill or reduces 99.9 of harmful bacteria/germs

Pump 2—3 times onto hand and rub adequately to make bubble
Apply over top of head and wipe with towel after use

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove.
Stop using and ask a doctor if rash occurs.

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Cocamidopropyl Betaine, Disodium EDTA, Methylparaben, Hydrolyzed Silk, Dimethicone Copolyol, Acorus Calamus Root Extract, Rosmarinus Officinalis (Rosemary) Extract, Dipotassium Glycyrrhizate, Lactobacillus/Aloe Barbadensis Ferment Filtrate, perfume, Water

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COCOBATH WATERLESS
benzalkonium chloride shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70072-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.19 g in 191.64 g

Ingredient Name	Strength
Inactive Ingredients
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLPARABEN (UNII: A2I8C7HI9T)
BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
ROSEMARY (UNII: IJ67X351P9)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70072-001-01	191.64 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/05/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/05/2015

Labeler - giod Co. (689514993)

Registrant - giod Co. (689514993)

Name	Address	ID/FEI	Business Operations
Establishment
giod Co.		689514993	manufacture(70072-001)