Label: BRIGHTON PROFESSIONAL ANTIBACTERIAL HAND SO AP- chloroxylenol liquid
- NDC Code(s): 49514-051-01, 49514-051-27
- Packager: Staples
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated December 22, 2020
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INGREDIENTS AND APPEARANCE
BRIGHTON PROFESSIONAL ANTIBACTERIAL HAND SO AP
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49514-051 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chloroxylenol (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) Chloroxylenol 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Coconut Acid (UNII: 40U37V505D) Oleic Acid (UNII: 2UMI9U37CP) Sodium Sulfate (UNII: 0YPR65R21J) MONOETHANOLAMINE (UNII: 5KV86114PT) COCO MONOETHANOLAMIDE (UNII: C80684146D) Coco-Betaine (UNII: 03DH2IZ3FY) Propylene Glycol (UNII: 6DC9Q167V3) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CORN OIL (UNII: 8470G57WFM) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49514-051-27 800 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/30/2006 12/31/2023 2 NDC:49514-051-01 3780 mL in 1 PACKAGE; Type 0: Not a Combination Product 04/30/2006 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/30/2006 Labeler - Staples (151064821)