MOONLITE ANTIBACTERIAL- benzalkonium chloride liquid

Moonlite Antibacterial by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride - 0.13%

PURPOSE

Purpose - Antiseptique(skin)cleanser

INDICATIONS & USAGE

Uses Effective in destorying(harmful) bacteria to provide antiseptic cleansing.

WARNINGS

Warning For external use only

STOP USE

Stop use and ask a doctor if irritation or redness develops

WHEN USING

When using the product

• avoid contact wiith 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

Direction

• Adults and children over 2 year
• For occasional and personal domestic use
• Supervise children when use this product
• Lather in hands with water for at least 30 seconds 
• Rinse well

OTHER SAFETY INFORMATION

• Store below 110F(43)
• May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT

Water,Lauramidopropylamine Oxide ( Triaminox LO ), Lauryl Glucoside, Citric Acid, PEG-150 distearate, Glycol Stearate, PEG-7 Glyceryl Cocoate,Cetrimonium Chloride, Tetrasodium EDTA,Isopropyl myristate, Aloe Leaf, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOONLITE ANTIBACTERIAL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-511
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
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
GLYCOL STEARATE (UNII: 0324G66D0E)
WATER (UNII: 059QF0KO0R)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
EDETATE SODIUM (UNII: MP1J8420LU)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-511-23	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/23/2020

Labeler - Brands International Corporation (243748238)

Registrant - Brands International Corporation (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International Corporation		243748238	manufacture(50157-511)