KLEENLINE ESSENTIALS ANTIBACTERIAL FOAMING HANDSOAP- benzalkonium chloride liquid

KleenLine Essentials Antibacterial Foaming HandSoap by

Drug Labeling and Warnings

KleenLine Essentials Antibacterial Foaming HandSoap by is a Otc medication manufactured, distributed, or labeled by Brady Industries, Betco Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

directions

Read entire label before using this product

Place enough product on your palms and rub thoroughly over all surfaces of both hands Rinse with clean water.

ingredients

water, Caprylyl/Capryl Glucoside, Tetrasodium EDTA, Glycerin, Sodium Benzoate, Fragrance, Citric Acid, FD&C Yellow 5, Aloe Barbadensis Leaf Juice, FD&C REd 40

INSTRUCTIONS FOR USE

Read teh entire label before using this product

Palce enough product on your palm and scrub thoroughly over all surfaces of both hands. Rinse with clean water

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

If swallowed, get medical help or Poison Control Center rgiht away.

PURPOSE

Antimicrobial

WARNINGS

For external use only, Do not ingest

When using this product avoid contact wiht eyes

Discontinue use if irritation or redness developes

If irritation pesists longer than 72 hours, consult a physician

DOSAGE & ADMINISTRATION

Place enough product on your palm and scrub thoroughlyover all surfaces of both hands. Rinse with clean water

INDICATIONS & USAGE

Antibacterial skin cleanser

use in a variety of publicfacilites including daycare centers, hospitals, nursing homes, phyicians offices and clinics

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KLEENLINE ESSENTIALS ANTIBACTERIAL FOAMING HANDSOAP 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79258-709
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GERANIOL (UNII: L837108USY)
ALLYL HEPTANOATE (UNII: AU4CYG9V68)
CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)
GLYCERIN (UNII: PDC6A3C0OX)
TETRASODIUM EDTA (UNII: MP1J8420LU)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
2-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 364FV60913)
2,6-DIMETHYLOCTAN-2-OL (UNII: EKV1VX27WR)
FD&C RED NO. 40 (UNII: WZB9127XOA)
ALCOHOL (UNII: 3K9958V90M)
4-CYCLOHEXYL-2-METHYL-2-BUTANOL (UNII: HFL24LW6V5)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRAL (UNII: T7EU0O9VPP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79258-709-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	12/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/16/2024

Labeler - Brady Industries (034932657)

Registrant - Betco Corporation (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation		005050158	manufacture(79258-709) , label(79258-709)