Label: SAFEGUARD ANTIBACTERIAL HAND WASH FRESH CLEAN SCENT- chloroxylenol liquid

  • NDC Code(s): 84126-008-45
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 5, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Chloroxylenol 0.35%

  • Purpose

    Antibacterial

  • Uses

    • For handwashing to decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    When using this product

    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
    • If irritation develops, stop use and consult a doctor.
    • Do not use as a facial wash

    Keep out of reach of children except under adult supervision

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    Turn pump to unlock.Wet hands. Apply 5 mL to hands and scrub thoroughly for 30 seconds. Rinse.

  • Inactive ingredients

    Water, sodium lauryl sulfate, cocamidopropyl betaine, citric acid, sodium chloride, fragrance, sodium citrate, sodium xylenesulfonate, benzyl alcohol, sodium benzoate, salicylic acid, disodium EDTA, PCA, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

  • Questions?

    1-800-595-1375

    www.safeguardna.com

  • Distr. by

    Procter & Gamble,

    Cincinnati, OH 45202

  • PRINCIPAL DISPLAY PANEL - 458 mL Label

    Safeguard ®

    Chloroxylenol
    Antibacterial

    Hand Wash

    enriched with skin conditioners

    Kills 99.9%

    of bacteria

    Fresh Clean Scent

    5.5 FL OZ 458 mL

    SFG

  • INGREDIENTS AND APPEARANCE
    SAFEGUARD ANTIBACTERIAL HAND WASH  FRESH CLEAN SCENT
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.35 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    PIDOLIC ACID (UNII: SZB83O1W42)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84126-008-45458 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/27/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/27/2024
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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