Label: DAWN ULTRA ANTIBACTERIAL HAND ORANGE SCENT- chloroxylenol soap

  • NDC Code(s): 37000-617-10, 37000-617-11, 37000-617-12, 37000-617-16, view more
    37000-617-19, 37000-617-20, 37000-617-21, 37000-617-22, 37000-617-23, 37000-617-26, 37000-617-38, 37000-617-40, 37000-617-47, 37000-617-53, 37000-617-54, 37000-617-57, 37000-617-59, 37000-617-63, 37000-617-65, 37000-617-70, 37000-617-82
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 9, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Chloroxylenol 0.30%

  • Purpose

    Antibacterial hand soap

  • Use

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only

    Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

  • Directions

    • wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.
  • Inactive ingredients

    Water, sodium lauryl sulfate, lauramine oxide, alcohol denat., phenoxyethanol, tetrasodium glutamate diacetate, sodiumchloride, fragrance, deceth-8, C9-11 alketh-8, PPG-26, sodium hydroxide, yellow 5, red 33

  • Questions?

    1-800-725-3296

  • SPL UNCLASSIFIED SECTION

    Distributed by PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 1.12L (1.18 QT) Bottle Label

    DAWN ®
    ULTRA

    CHLOROXYLENOL ANTIBACTERIAL HAND SOAP


    ORANGE SCENT

    *VS DAWN NON-CONCENTRATED


    DISHWASHING LIQUID

    1.12L (1.18 QT) 38 FL OZ

    Dawn

  • INGREDIENTS AND APPEARANCE
    DAWN ULTRA ANTIBACTERIAL HAND  ORANGE SCENT
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-617
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    DECETH-8 (UNII: 19FQ96EA8Q)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PPG-26 (UNII: V86KZL3H2Z)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    C9-11 PARETH-8 (UNII: 80E6PSE1XL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-617-26266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201401/10/2018
    2NDC:37000-617-59591 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201401/10/2018
    3NDC:37000-617-63638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201412/12/2019
    4NDC:37000-617-70709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201401/10/2018
    5NDC:37000-617-101010 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201412/12/2019
    6NDC:37000-617-111120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201401/10/2018
    7NDC:37000-617-161660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/201408/01/2024
    8NDC:37000-617-23236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/10/201702/01/2021
    9NDC:37000-617-53532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/10/201712/12/2019
    10NDC:37000-617-222210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/10/201701/01/2022
    11NDC:37000-617-47479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/201812/01/2021
    12NDC:37000-617-57573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/201802/01/2025
    13NDC:37000-617-121210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/201804/01/2021
    14NDC:37000-617-82828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/2018
    15NDC:37000-617-20207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/02/201902/01/2024
    16NDC:37000-617-401200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/02/201912/01/2023
    17NDC:37000-617-19192 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/202109/01/2024
    18NDC:37000-617-381120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2021
    19NDC:37000-617-21221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/202211/01/2025
    20NDC:37000-617-54532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/07/202310/01/2025
    21NDC:37000-617-65650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/07/2014
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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