Label: CVS PHARMACY QUICK RELIEF- zinc oxide cream

  • Category: HUMAN OTC DRUG LABEL

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 January 8, 2020

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  • ACTIVE INGREDIENT

    Active Ingredient

    Zinc Oxide, 13.0%

  • PURPOSE

    Purpose

    Skin protectant

  • INDICATIONS & USAGE

    Uses

    • helps treat and prevent diaper rash
    • protects chafed skin due to diaper rash and helps seal out wetness
  • WARNINGS

    Warnings

    For external use only.

    When using this product  -do not get into eyes

    Stop use and ask a doctor if -condition worsens

    -symptoms last more than 7 days or clear up and occur again

    within a few days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical

    help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    -change wet and soiled diapers promptly  -cleanse the

    diaper area  -allow to dry  -apply cream liberally as often

    as necessary, with each diaper change, especially at

    bedtime or at any time when exposure to wet diapers may

    be prolonged

  • STORAGE AND HANDLING

    Other Information

    -store at 20 to 25 C

    (68 to 77 F)

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Aloe Barbadensis Leaf Juice,

    Beeswax, Dimethicone,

    Dipolyhydroxystearate,

    Fragrance, Magnesium Sulfate,

    Methylparaben, Mineral Oil,

    PEG-30 Microcrystalline Wax,

    Petrolatum, Phenoxyethanol,

    Polyglycerol-3 Diistearate,

    Potassium Hydroxide,

    Propylparaben, Sorbitan

    Sesquioleate, Tocopheryl

    Acetate (Vitamin E), Water

  • PRINCIPAL DISPLAY PANEL

    copy of label

  • INGREDIENTS AND APPEARANCE
    CVS PHARMACY  QUICK RELIEF
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-728
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.013 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-728-151 in 1 CARTON05/01/2015
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34705/01/2015
    Labeler - CVS Pharmacy (062312574)
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