Label: NATURES CURE BODY ACNE TREATMENT- salicylic acid spray

  • 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 30, 2019

If you are a consumer or patient please visit this version.

  • Drug Facts

    Active ingredient

    Salicylic Acid 2.0%

  • PURPOSE

    Purpose

    Acne Treatment

  • INDICATIONS & USAGE

    Uses

    * treats acne * clears acne blemishes * helps prevent new acne pimples

  • WARNINGS AND PRECAUTIONS

    Warnings

    For external use only

    Warnings

    For external use only

  • WHEN USING

    When using this product

    * Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.

    * Do not spray directly on or near face.

    * Avoid contact with eyes, lips and mouth.

  • 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 * Cleanse skin thoroughly.

    *Spray the entire affected area with a thin layer 1 to 3 times daily.

    *Because excessive drying of the skin may occur, gradually increase to 2 or 3 times daily if needed or as directed by a doctor.

    * Leave on all day or night.

    * If bothersome dryness or peeling occurs, reduce usage to once a day or every other day.

    * To use on face, spray onto cotton ball and brush onto skin.

  • DESCRIPTION

    Nature's Cure clears and prevents acne on your back, chest, neck and arms. The maximum strength formula sprays from any angle, even upside down, to treat hard-to-reach places. It fights acne caused by sweating and friction from athletic gear and clothing. The non-staining spray contains moisturizing botanicals that help soothe skin.

  • INACTIVE INGREDIENT

    Allantoin, Aloe Barbadensis Leaf Juice, Arctium Majus Root Extract (Burdock), Calendula Officinalis Flower Extract, Capryloyl Glycine, Chamomilla Recutita (Matricaria) Flower Extract, Cinnamomum Zeylanicum Bark Water Extract, Fragrance, Hamamelis Virginiana (Witch Hazel) Extract, Methylparaben, Phospholipids, Propylene Glycol, Propylparaben, Salix Nigra (Willow) Bark Extract, Sarcosine, SD Alcohol 40, Sodium Citrate, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).

  • QUESTIONS

    Call toll free 1-877-4MYZITS(USA only)

    or visit www.naturescure.com

  • PRINCIPAL DISPLAY PANEL

    AB-1914

  • INGREDIENTS AND APPEARANCE
    NATURES CURE BODY ACNE TREATMENT 
    salicylic acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21839-680
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    WATER (UNII: 059QF0KO0R)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALCOHOL (UNII: 3K9958V90M)  
    SARCOSINE (UNII: Z711V88R5F)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21839-680-01103 mL in 1 BOTTLE; Type 0: Not a Combination Product06/20/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D06/20/2016
    Labeler - Gordon Laboratories, Inc. (008328619)
    Registrant - Gordon Laboratories, Inc. (008328619)
    Establishment
    NameAddressID/FEIBusiness Operations
    GORDON LABORATORIES, INC008328619manufacture(21839-680)