COCOBATH WATERLESS- benzalkonium chloride shampoo

Cocobath Waterless by

Drug Labeling and Warnings

Cocobath Waterless by is a Otc medication manufactured, distributed, or labeled by giod Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

PURPOSE

Antibacterial

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

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

WARNINGS

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 CHILDREN

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

COCOBATH WATERLESS 
benzalkonium chloride shampoo

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

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

Labeler - giod Co. (689514993)

Registrant - giod Co. (689514993)

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