Label: ANTIBACTERIAL MOISTURIZING LAVENDER VANILLA ALOE AND VITAMIN E- benzalkonium chloride liquid
- NDC Code(s): 50157-517-10, 50157-517-23, 50157-517-37, 50157-517-44
- Packager: Brands International Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 27, 2021
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL MOISTURIZING LAVENDER VANILLA ALOE AND VITAMIN E
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50157-517 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) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50157-517-37 3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/26/2021 2 NDC:50157-517-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/26/2021 3 NDC:50157-517-23 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/26/2021 4 NDC:50157-517-44 443 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(50157-517)