Label: DAYLOGIC ANTIBACTERIAL GOLD REFILL- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-2953-2 - Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 6, 2016
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INGREDIENTS AND APPEARANCE
DAYLOGIC ANTIBACTERIAL GOLD REFILL
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-2953 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) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) GLYCERIN (UNII: PDC6A3C0OX) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) COCO MONOETHANOLAMIDE (UNII: C80684146D) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-2953-2 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/05/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/05/2016 Labeler - Rite Aid Corporation (014578892) Registrant - Apollo Health and Beauty Care (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care 201901209 manufacture(11822-2953)