Label: EMERGENCY ZIT STICK ACNE TREATMENT- salicylic acid stick 

  • Label RSS
  • NDC Code(s): 61084-125-01, 61084-125-02
  • Packager: Basic Research
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 04/14

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  • ACTIVE INGREDIENT

    Active ingredient             Purpose

    Salicylic Acid 2%           Acne Treatment Cream

    Uses

    Treats acne

    Clears up acne blemishes

    Penetrates Pores to clear most acne pimples

    Keep out of reach of children. If swallowed get medical or contact a Poison Control Center right away. If swallowed get medical help or contact a poison control center right away.

    Do not use on broken skin or apply to large areas of the body

    Warnings

    For external use only

    Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. if this occurs only one medication should be used unless directed by a physician.

    Apply to effected areas only

    Directions

    Cleanse the skin thoroughly before applying this medication.

    Cover the entire affected area with a thin layer one to three times daily.

    Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three time daily if needed or as directed by a doctor.

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

    Inactive ingredients

    Water (Aqua), Butylene Glycol, Cetearyl Alcohol, Cetyl Alcohol, Glycerin, Steareth-2, Oleth-10, Caprylic/Capric Triglyceride, Octyldodecanol, Caprylyl Methicone,Bakuchiol, Hydrolyzed Optunia Ficus-Indica Flower Extract, Boerhavia Diffusia Root Extract, Allantoin, Sodium Hyaluronate, Dicetyl Phophate, C18-21 Alkane, Hydroxyethyl Acrylate/sodium Acryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Xanthan Gum, Glyceryl Acrylate/Acrylic Acid Copolymer, Squalane, Ethylhexylglycerin, Polysorbate 60, Polyisobutene, Ceteth-10 Phosphate, Disodium EDTA, Bisabolol, PVM/MA Copolymer, Phenoxyethanol, Sodium Hydroxide, Magnesium Aluminum Silicate, Tocopheryl Acetate, Sodium Benzoate, Titanium Dioxide (CI 77891)

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  • PRINCIPAL DISPLAY PANEL

    Emergency Zit StickTM
    Acne Treatment

    " I always keep one in my purse"

    .07 fl.oz. [2 ml]

    Box label

    Primary

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  • INGREDIENTS AND APPEARANCE
    EMERGENCY ZIT STICK  ACNE TREATMENT
    salicylic acid stick
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:61084-125
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 2 g  in 2 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    BUTYLENE GLYCOL  
    CETOSTEARYL ALCOHOL  
    CETYL ALCOHOL  
    GLYCERIN  
    STEARETH-2  
    OLETH-10  
    MEDIUM-CHAIN TRIGLYCERIDES  
    OCTYLDODECANOL  
    CAPRYLYL TRISILOXANE  
    BAKUCHIOL  
    ALLANTOIN  
    HYALURONATE SODIUM  
    DIHEXADECYL PHOSPHATE  
    C18-C21 ALKANE  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)  
    CAPRYLYL GLYCOL  
    XANTHAN GUM  
    SQUALANE  
    ETHYLHEXYLGLYCERIN  
    POLYSORBATE 60  
    POLYISOBUTYLENE (1300 MW)  
    CETETH-10 PHOSPHATE  
    EDETATE DISODIUM  
    LEVOMENOL  
    PHENOXYETHANOL  
    SODIUM HYDROXIDE  
    MAGNESIUM ALUMINUM SILICATE  
    .ALPHA.-TOCOPHEROL ACETATE  
    SODIUM BENZOATE  
    TITANIUM DIOXIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61084-125-02 1 in 1 CARTON
    1 NDC:61084-125-01 2 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 11/05/2013
    Labeler - Basic Research (805947405)
    Registrant - Wasatch product Development (962452533)
    Establishment
    Name Address ID/FEI Business Operations
    Wasatch product Development 962452533 manufacture(61084-125)
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