ANTIBACTERIAL- benzalkonium chloride 0.13% liquid

Antibacterial by

Drug Labeling and Warnings

Antibacterial by is a Otc medication manufactured, distributed, or labeled by Flex Beauty Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Purpose - Antibacterial

INDICATIONS & USAGE

Use help eliminate bacteria on hands

Warnings 

For external use only

STOP USE

Stop use and ask a doctor if irritation or redness develops

When using this product

Avoid contact with eyes.In case of contact, flush and rinse with water.

Keep out of reach of children

Except under adult supervision. 

If swallowed get medical help or contact posion control right away.

Directions

Wash hands and rinse

INACTIVE INGREDIENT

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Coamide Methyl MEA, Fragrance, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, DMDM Hydantoin ,Cl 17200, Cl 19140.

ACTIVE INGREDIENT

Benzalkonium Chloride - 0.13%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL 
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72308-016
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
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
DMDM HYDANTOIN (UNII: BYR0546TOW)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72308-016-01	325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020

Labeler - Flex Beauty Labs (080858917)