Label: HIGHMARK PROFESSIONAL GOLD AND CLEAN ANTIMICROBIAL LTN SP- chloroxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 61139-421-10, 61139-421-20, 61139-421-80, 61139-421-89, view more61139-421-90 - Packager: Office Max, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 22, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Directions
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Inactive Ingredients
Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Aloe Barbadensis Leaf Juice, Cocamide MEA, Coco-Betaine, Hydrolyzed Vegetable Protein, Propylene Glycol, Retinyl Palmitate, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Hydroxypropyl Methylcellulose, Fragrance (Parfum)
- PRINCIPAL DISPLAY PANEL
- Warnings
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INGREDIENTS AND APPEARANCE
HIGHMARK PROFESSIONAL GOLD AND CLEAN ANTIMICROBIAL LTN SP
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61139-421 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) 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) HYPROMELLOSES (UNII: 3NXW29V3WO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61139-421-80 800 mL in 1 BAG 2 NDC:61139-421-89 1200 mL in 1 BOTTLE 3 NDC:61139-421-90 1250 mL in 1 BOTTLE 4 NDC:61139-421-10 1000 mL in 1 BOTTLE 5 NDC:61139-421-20 2000 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/22/2013 Labeler - Office Max, Inc. (009073099)
