HOBOCO AND CO FRESH EUCALYPTUS- benzalkonium chloride liquid liquid

HOBOCO AND CO FRESH EUCALYPTUS by

Drug Labeling and Warnings

HOBOCO AND CO FRESH EUCALYPTUS by is a Otc medication manufactured, distributed, or labeled by HOME & BODY COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%. Purpose : Antibacterial

PURPOSE

Antibacterial

Use

Help eliminate bacteria on hands

WARNINGS

For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

Keep out of reach of children

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

DIRECTIONS

Wash hands and rinse

INACTIVE INGREDIENTS

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Sodium Benzoate, Phenoxyethanol, Polysorbate 20, Fragrance, Glycerin

DOSAGE & ADMINISTRATION

PRODUCT LABEL

INGREDIENTS AND APPEARANCE

HOBOCO AND CO FRESH EUCALYPTUS 
benzalkonium chloride liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73746-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73746-012-01	724 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/14/2020

Labeler - HOME & BODY COMPANY (081290720)

Registrant - HOME & BODY COMPANY (081290720)

Establishment
Name	Address	ID/FEI	Business Operations
HOME & BODY COMPANY		081290720	manufacture(73746-012)