Label: CVS PHARMACY DANDRUFF- pyrithione zinc liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 6, 2013

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  • ACTIVE INGREDIENT

    PYRITHIONE ZINC 1%

    PURPOSE

    ANTIDANDRUFF

  • USES

    TO HELP PREVENT RECURRENCE OF FLAKING AND ITCHING 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

    IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

  • DIRECTIONS

    SHAKE WELL. FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRED

  • QUESTIONS/COMMENTS?

    1-800-746-7287

  • INACTIVE INGREDIENTS

    WATER (AQUA), AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, GLYCERIN, GLYCOL DISTEARATE, COCAMIDE MEA, CETYL ALCOHOL, FRAGRANCE (PARFUM), ALOE BARBADENSIS LEAF JUICE, DIMETHICONE, TOCOPHERYL ACETATE, PANTHENOL, ACETAMIDOPROPYL TRIMONIUM CHLORIDE, LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, PEG-3 DIOLEOYLAMIDOETHYLMONIUM METHOSULFATE, DIMETHICONOL, SODIUM LAURYL GLUCOSE CARBOXYLATE, LAURYL GLUCOSIDE, AMODIMETHICONE, HYDROXYPROPYL METHYLCELLULOSE, SODIUM DODECYLBENZENESULFONATE, LAURETH-9, DMDM HYDANTOIN, C11-15 PARETH-7, TRIDECETH-12, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, HYDROXYETHYLCELLULOSE, BLUE 1 (CI 42090)

  • LABEL COPY

    IMAGE OF THE LABEL

  • INGREDIENTS AND APPEARANCE
    CVS PHARMACY  DANDRUFF
    pyrithione zinc liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-428
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ACETAMIDOPROPYL TRIMONIUM CHLORIDE (UNII: 2SQT0WU9CO)  
    LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)  
    PEG-3 DISTEAROYLAMIDOETHYLMONIUM METHOSULFATE (UNII: 395MHJ5PUR)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    AMODIMETHICONE (3500 CST) (UNII: 42AFE8JAOY)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    LAURETH-9 (UNII: 0AWH8BFG9A)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    C11-15 PARETH-7 (UNII: 261HPE0IS3)  
    TRIDECETH-12 (UNII: YFY3KG5Y7O)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-428-11325 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H12/05/2013
    Labeler - CVS PHARMACY (062312574)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(59779-428)
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