Label: DANDRENE ANTI-DANDRUFF CONDITIONER- zinc pyrithione lotion

  • NDC Code(s): 69188-300-07
  • Packager: DS Healthcare Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 8, 2024

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  • Active ingredient

    Zinc Pyrithione 1%

  • Purpose

    Anti-dandruff

  • Uses

    Relieves and helps prevent recurrence of scalp itch, irritation, redness, flaking and scaling associated with dandruff 

  • Warnings

    For external use only. 

    When using this Product: Avoid contact with eyes, If contact occurs, rinse eyes thoroughly with water

    Stop use and ask a doctor if  Condition worsens or does not improve after regular use of this product as directed

    Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Apply to wet hair and scalp with gentle massage, leave in for 2 minutes, rinse 

    For best results use atleast 2 times per week or as direacted by a doctor

    For maximum benefits use 4-5 times a week along with Dandrene anti-dandruff shampoo

  • Inactive ingredients

    WATER, CETEARYL ALCOHOL, BEHENTRIMONIUM CHLORIDE, CETYL ESTERS, ALOE VERA GEL, KERATIN, HYDROLYZED KERATIN, AMODIMETHICONE, PEPPERMINT OIL, POLYSILICONE-15, MENTHOL, CETRIMONIUM CHLORIDE, SD ALCOHOL 40-B, DISODIUM EDTA, TRIDECETH-12, CAPRYLYL GLYCOL, METHYLISOTHIAZOLINONE

  • Product label

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  • INGREDIENTS AND APPEARANCE
    DANDRENE ANTI-DANDRUFF CONDITIONER 
    zinc pyrithione lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69188-300
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    KERATIN, TYPE I CYTOSKELETAL 40 (UNII: 2QD5SI65D8)  
    HYDROLYZED SHEEP WOOL KERATIN (200 MW) (UNII: R6K7AW17SU)  
    AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    POLYSILICONE-15 (UNII: F8DRP5BB29)  
    MENTHOL (UNII: L7T10EIP3A)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    ALCOHOL (UNII: 3K9958V90M)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    TRIDECETH-12 (UNII: YFY3KG5Y7O)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69188-300-07205 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/20/2016
    Labeler - DS Healthcare Group, Inc. (015504134)
    Establishment
    NameAddressID/FEIBusiness Operations
    A.I.G. Technologies, Inc086365223manufacture(69188-300)
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