Label: CLOROX ANTIBACTERIAL HAND - CITRUS BLOSSOM- chloroxylenol soap
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Contains inactivated NDC Code(s)
NDC Code(s): 69540-0078-1 - Packager: Brand Buzz
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 January 5, 2016
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive Ingredients
WATER (AQUA, EAU), SODIUM LAURETH SULFATE, PEG-4 RAPESEEDAMIDE, PANTHENOL, TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, COCAMIDOPROPYL BETAINE, PEG-150 DISTEARATE, POLYSORBATE 20, GLYCERIN, ASCORBIC ACID, BIOTIN, NIACINAMIDE, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, TETRASODIUM EDTA, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FRAGRANCE (PARFUM), RED 40 (CI 16035), YELLOW 6 (CI 15985), LIMONENE
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label
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INGREDIENTS AND APPEARANCE
CLOROX ANTIBACTERIAL HAND - CITRUS BLOSSOM
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69540-0078 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol 0.003 g in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Sodium Laureth-3 Sulfate (UNII: BPV390UAP0) PEG-4 Rapeseedamide (UNII: 89575CN928) Panthenol (UNII: WV9CM0O67Z) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Sheanut Oil (UNII: O88E196QRF) Coconut (UNII: 3RT3536DHY) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) PEG-150 Distearate (UNII: 6F36Q0I0AC) Polysorbate 20 (UNII: 7T1F30V5YH) Glycerin (UNII: PDC6A3C0OX) Ascorbic Acid (UNII: PQ6CK8PD0R) Biotin (UNII: 6SO6U10H04) Niacinamide (UNII: 25X51I8RD4) Propylene Glycol (UNII: 6DC9Q167V3) Sodium Chloride (UNII: 451W47IQ8X) Citric Acid Monohydrate (UNII: 2968PHW8QP) PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794) Sodium Hydroxide (UNII: 55X04QC32I) Edetate Sodium (UNII: MP1J8420LU) Methylchloroisothiazolinone (UNII: DEL7T5QRPN) Methylisothiazolinone (UNII: 229D0E1QFA) FD&C Red NO. 40 (UNII: WZB9127XOA) FD&C Yellow NO. 6 (UNII: H77VEI93A8) Product Characteristics Color ORANGE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69540-0078-1 295.735 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 02/01/2016 Labeler - Brand Buzz (079266204)