Label: 111MEDCO MEDICATED BAR 2 PYRITHIONE ZINC- pyrithione zinc soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2023

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  • Drug Facts

  • Active ingredient

    Pyrithione Zine 2%

    Purpose

    Dandruff/Seborrheic Dermatitis

  • Uses

    • For relief of skin itching, flaking, and scaling associated with dandruff and seborrheic dermatitis
  • Warnings

    For external use only

    When using this product

    • skin irritation and dryness may occur if you use other topical acne medications at the same time or immediately following use of this product. If this occurs, use only one medication at a time unless directed by a healthcare provider.

    Keep out of reach of children.

    If swallowed, get medial help or contact a Poison Control Center right away.

  • Directions

    • Use on affected areas in place of your  regular soap
    • For best results use at least twice a week or as directed by your healthcare provider
  • Inactive ingredients

    Sodium palmate, sodium cocoate*, sodium palm kernelate*, agua, glycerin, orange extract, sodium chloride, pentasodium pentetate. (*may contain this ingredient)

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    111MEDCO MEDICATED BAR 2 PYRITHIONE ZINC 
    pyrithione zinc soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72811-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM COCOATE (UNII: R1TQH25F4I)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72811-002-04113 g in 1 CARTON; Type 0: Not a Combination Product10/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03210/01/2023
    Labeler - 111MedCo LLC (065115643)
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