ANTIBACTERIAL COCONUT WATER ALOE AND VITAMIN E- benzalkonium chloride liquid

Antibacterial by

Drug Labeling and Warnings

Antibacterial by is a Otc medication manufactured, distributed, or labeled by Brands International Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride - 0.13%

PURPOSE

Purpose - Antiseptic Skin cleanser

INDICATIONS & USAGE

Effective in destroying (harmful) bacteria to provide antiseptic cleansing

WARNINGS

Warnings For external use only

STOP USE

Stop use and ask a doctor if irritation or redness develops

WHEN USING

When using this product

• avoid contact with eyes. 
• If contact occurs, rinse eye thoroughly with water

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children :

• If swallowed get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions:

• For occasional and personal domestic use
• Supervise children when they use this product.
• Lather in hands with water for at least 30 seconds.
• Rinse well.

INACTIVE INGREDIENT

Lauramidopropylamine oxide, Lauryl Glucoside, PEG-150 distearate, Glycol Stearate, Perfume, PEG-7 glycerly cocoate, Cetrimonium Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Isopropyl myristate, Tocopheryl Acetate

OTHER SAFETY INFORMATION

• Store below 59F-86F
• May discolor certain fabrics or surfaces.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL  COCONUT WATER ALOE AND VITAMIN E
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-516
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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCOL STEARATE (UNII: 0324G66D0E)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-516-37	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/26/2021
2	NDC: 50157-516-10	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/26/2021
3	NDC: 50157-516-23	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/26/2021
4	NDC: 50157-516-44	443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/26/2021

Labeler - Brands International Corporation (243748238)

Registrant - Brands International Corporation (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International Corporation		243748238	manufacture(50157-516)