Label: 28.5% SALICYLIC ACID- salicylic acid solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 6, 2018

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

  • 28.5% Salicylic Acid Extended Release Antiviral Film-Forming Solution: Package Insert

    Rx only

    FOR TOPICAL USE ONLY.

    NOT FOR OPHTHALMIC, ORAL OR INTRAVAGINAL USE.

    DESCRIPTION

    This Product is a topical preparation containing 28.5% salicylic acid extended release in a proprietary film-forming virucidal solution composed of acrylates copolymer, butyl acetate, carthamus tinctorius seed oil, cocamidopropyl dimethylamine, ethylhexylglycerin, isopropyl alcohol, isopropyl-metacresol, olea europaea fruit oil, phenic acid, phenoxyethanol, polysorbate 80, polyvinyl butyral, trimethyl pentanyl diisobutyrate, and water. The pharmacologic activity of the Product is generally attributed to the keratolytic activity of salicylic acid, which is incorporated into a polyacrylic, film-forming virucidal solution designed to cover the wart without the need for a bandage. The structural formula of salicylic acid is:

    5-01.jpg

    CLINICAL PHARMACOLOGY

    Although the exact mode of action for salicylic acid in the treatment of warts is unknown, its activity appears to be associated with its keratolytic action, which results in mechanical removal of epidermal cells infected with wart viruses. This Product incorporates a unique patented extended release form of salicylic acid that provides for enhanced release of salicylic acid for over 24 hours.

    The virucidal complex incorporated into this Products proprietary solution is designed to help reduce risk of reinfection at the wart site, as well as prevent viral contamination of the product under normal usage.

    INDICATIONS AND USAGE

    This Product is indicated for the topical treatment and removal of common warts and plantar warts.

    CONTRAINDICATIONS

    Patients with diabetes or impaired blood circulation should not use the Product. This Product also should not be used on moles, birthmarks, and unusual warts with hair growing from them, or warts on the face.

    PRECAUTIONS

    This Product is for external use only. Do not permit it to contact eyes or mucous membranes. If contact with eyes or mucous membranes occurs, immediately flush with water for 15 minutes. The Product should not be allowed to contact normal skin surrounding the wart site, since localized irritation may occur. Treatment should be discontinued if excessive irritation occurs.

    The Product is flammable. Keep away from fire or flame. Keep bottle tightly capped when not in use.

    ADVERSE REACTIONS

    A localized irritant reaction may occur if this Product is applied to the normal skin surrounding the wart. Any irritation may normally be controlled by temporarily discontinuing use and by applying the medication only to the wart site when treatment is resumed.

    DOSAGE AND ADMINISTRATION

    Prior to applying the Product, soak wart in warm water for five minutes. Remove any loose tissue by gently rubbing with a washcloth, emery board, or pumice stone. Dry the wart site thoroughly. Using the brush applicator supplied, apply it twice to the entire wart surface, allowing the first application to dry before applying the second. Continue treatment once or twice a day as directed by your healthcare provider. Be careful not to apply to surrounding skin.

    Clinically visible improvement normally occurs during the first or second week of therapy. Resolution may be expected after four to six weeks of the Product use, though some warts may take longer to remove.

    HOW SUPPLIED

    This Product is supplied in 10 mL amber bottles with a brush applicator (NDC 42783-324-10).

    Store at 15° to 30°C (59° to 86°F).

    Manufactured for:

    Elorac, Inc.

    Vernon Hills, IL 60061

    U.S. Patent No. 6,979,440

    Additional Patent Pending

    © 2014 Elorac, Inc.

    1/2018

    211909

    PATIENT INSTRUCTIONS

    Your health care provider has prescribed this Product, a topical prescription preparation for the treatment of common warts and plantar warts. In order for it to work properly and to ensure maximum benefit, the following instructions should be followed carefully. Of course, as with any medication, always consult your health care provider if you experience any discomfort or unexpected reactions.

    STEP 1

    WASH

    • Soak wart area in warm water for about 5 minutes.
    • Remove any loose tissue using a washcloth, emery board, or pumice stone.
    • Dry thoroughly.

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    STEP 2

    BRUSH

    • Using the brush applicator supplied, apply twice to entire wart surface, allowing the first application to dry before applying the second.
    • Be careful not to apply to surrounding skin.
    • Leave the Product on wart area after it dries.

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    Repeat Step 1 and Step 2 once or twice daily as advised by the health care provider.

    Clinically visible improvement will normally occur during the first or second week of therapy. Resolution may be expected after four to six weeks of the Product use, though some warts may take longer to remove.

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    Vernon Hills, IL 60061

  • 28.5% Salicylic Acid Extended Release Antiviral Film-Forming Solution:  Container Label Principal Display Panel

    NDC 42783-324-10

    28.5% Salicylic Acid Extended Release Antiviral Film-Forming Solution

    1/3 fl. oz. (10 mL)

    Rx only

    bottle-label.jpg

  • 28.5% Salicylic Acid Extended Release Antiviral Film-Forming Solution: Carton Label Principal Display Panel

    NDC 42783-324-10

    28.5% Salicylic Acid Extended Release Antiviral Film-Forming Solution

    1/3 fl. oz. (10 mL)

    Rx only

    carton-label.jpg

  • INGREDIENTS AND APPEARANCE
    28.5% SALICYLIC ACID 
    salicylic acid solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:42783-324
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    salicylic acid (UNII: O414PZ4LPZ) (salicylic acid - UNII:O414PZ4LPZ) salicylic acid285 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42783-324-101 in 1 CARTON04/30/2018
    110 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/30/2018
    Labeler - Elorac, Inc. (832590009)
    Registrant - Elorac, Inc. (832590009)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933manufacture(42783-324) , analysis(42783-324) , pack(42783-324) , label(42783-324)