Label: WAXIE ANTIBACTERIAL HAND- chloroxylenol soap
- NDC Code(s): 61666-901-23, 61666-901-41
- Packager: Waxie's Enterprises, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 19, 2025
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warning:
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive ingredients
Water (aqua) (7732-18-5), Sodium Lauryl Sulfate (68585-47-7), Cocamidopropyl Hydroxysultaine (68139-30-0), Propylene Glycol (57-55-6), Sodium Chloride (7647-14-5), Propanediol (26264-14-2), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycol Distearate (627-83-8), Fragance (Proprietary), Sodium Polyitaconate (26099-89-8), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Acid Red 51 (16423-68-0).
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
WAXIE ANTIBACTERIAL HAND
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61666-901 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 2.5 g in 1 L Inactive Ingredients Ingredient Name Strength ACID RED 51 (UNII: PN2ZH5LOQY) 2-BROMO-2-NITROPROPANE-1,3-DIOL (UNII: 6PU1E16C9W) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) FRAGRANCE 13576 (UNII: 5EM498GW35) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED) (UNII: G7SW5QN7TT) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) GLYCOL DISTEARATE (UNII: 13W7MDN21W) Product Characteristics Color pink (Pearly) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61666-901-41 3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/02/2021 2 NDC:61666-901-23 0.47 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/02/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 12/02/2021 Labeler - Waxie's Enterprises, LLC (029142577)

