Label: CLOROX ANTIBACTERIAL HAND - WILD LAVENDER AND VANILLA- chloroxylenol soap
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Contains inactivated NDC Code(s)
NDC Code(s): 69540-0075-1 - 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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- 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), EXT. VIOLET 2 (CI 60730), RED 33 (CI 17200), ALPHA-ISOMETHYL IONONE, BUTYLPHENYL METHYLPROPIONAL
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label
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INGREDIENTS AND APPEARANCE
CLOROX ANTIBACTERIAL HAND - WILD LAVENDER AND VANILLA
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69540-0075 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) EXT. D&C Violet NO. 2 (UNII: G5UX3K0728) D&C Red NO. 33 (UNII: 9DBA0SBB0L) Isomethyl-.Alpha.-Ionone (UNII: 9XP4LC555B) Butylphenyl Methylpropional (UNII: T7540GJV69) Product Characteristics Color PURPLE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69540-0075-1 295.735 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)