Label: MOONLITE ANTIBACTERIAL- benzalkonium chloride liquid
- NDC Code(s): 50157-511-23
- Packager: Brands International Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated September 23, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
MOONLITE ANTIBACTERIAL
benzalkonium chloride liquidProduct 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)