Label: HYDROCORTISONE AND ACETIC ACID- hydrocortisone and acetic acid otic solution

  • NDC Code(s): 71656-064-10
  • Packager: Saptalis Pharmaceuticals, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application Authorized Generic

Drug Label Information

Updated April 25, 2025

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  • DESCRIPTION

    DESCRIPTION:Hydrocortisone and Acetic Acid Otic Solution, USP is a solution containing hydrocortisone (1%) and acetic acid (2%), in a propylene glycol vehicle containing benzethonium chloride (0.02%), citric acid (0.05%), propylene glycol diacetate (3%) and sodium acetate (0.015%). The empirical formulas for acetic acid and hydrocortisone are CH3COOH, and C21H30O5, with a molecular weight of 60.05 and 362.46, respectively. The structural formulas are:

    Chemical Structure_Hydrocortisone

    Hydrocortisone and Acetic Acid is available as a nonaqueous otic solution buffered at pH 3 for use in the external ear canal.

  • CLINICAL PHARMACOLOGY

    CLINICAL PHARMACOLOGY:Acetic acid is antibacterial and antifungal; hydrocortisone is antiinflammatory, antiallergic and antipruritic; propylene glycol is hydrophilic and provides a low surface tension; benzethonium chloride is a surface active agent that promotes contact of the solution with tissues.

  • INDICATIONS & USAGE

    INDICATIONS AND USAGE:For the treatment of superficial infections of the external auditory canal caused by organisms susceptible to the action of the antimicrobial, complicated by inflammation.

  • CONTRAINDICATIONS

    CONTRAINDICATIONS:Hypersensitivity to Hydrocortisone and Acetic Acid or any of the ingredients; herpes simplex, vaccinia and varicella. Perforated tympanic membrane is considered a contraindication to the use of any medication in the external ear canal.

  • WARNINGS

    WARNINGS:Discontinue promptly if sensitization or irritation occurs.

  • PRECAUTIONS

    PRECAUTIONS: Transient stinging or burning may be noted occasionally when the solution is first instilled into the acutely inflamed ear.

    PEDIATRIC USE:Safety and effectiveness in pediatric patients below the age of 3 years have not been established.

  • ADVERSE REACTIONS

    ADVERSE REACTIONS:Stinging or burning may be noted occasionally; local irritation has occurred very rarely.

    To report SUSPECTED ADVERSE REACTIONS, contact Saptalis Pharmaceuticals, LLC at 1-833-727-8254 or FDA at 1-­800-FDA-1088 or www.fda.gov/medwatch.

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION:Carefully remove all cerumen and debris to allow Hydrocortisone and Acetic Acid to contact infected surfaces directly. To promote continuous contact, insert a wick of cotton saturated with Hydrocortisone and Acetic Acid into the ear canal; the wick may also be saturated after insertion. Instruct the patient to keep the wick in for at least 24 hours and to keep it moist by adding 3 to 5 drops of Hydrocortisone and Acetic Acid every 4 to 6 hours. The wick may be removed after 24 hours but the patient should continue to instill 5 drops of Hydrocortisone and Acetic Acid 3 or 4 times daily thereafter, for as long as indicated. In pediatric patients, 3 to 4 drops may be sufficient due to the smaller capacity of the ear canal.

  • HOW SUPPLIED

    HOW SUPPLIED:Hydrocortisone and Acetic Acid Otic Solution, USP, containing hydrocortisone (1%) and acetic acid (2%), is available in 10 mL, measured-drop, safety-tip plastic bottles (NDC 71656-064-10).

  • SPL UNCLASSIFIED SECTION

    STORAGE:Store at room temperature, 20°C to 25°C (68°F to 77°F). Keep container tightly closed.

    Rx only

    Distributed by:
    Saptalis Pharmaceuticals, LLC.
    Hauppauge, NY 11788

    MADE IN USA

    May 2024-R3
    PPM-0082

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    NDC 71656-064-10

    Hydrocortisone and Acetic Acid Otic Solution, USP

    1% / 2%

    For Otic Use Only

    Rx only

    10 mL

    Label

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    NDC 71656-064-10

    Hydrocortisone and Acetic Acid Otic Solution, USP

    1% / 2%

    For Otic Use Only

    Rx only

    10 mL

    Carton

  • INGREDIENTS AND APPEARANCE
    HYDROCORTISONE AND ACETIC ACID 
    hydrocortisone and acetic acid otic solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:71656-064
    Route of AdministrationAURICULAR (OTIC)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETIC ACID (UNII: Q40Q9N063P) (ACETIC ACID - UNII:Q40Q9N063P) ACETIC ACID20.75 mg  in 1 mL
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10.375 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLENE GLYCOL DIACETATE (UNII: 5Z492UNF9O)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71656-064-101 in 1 CARTON02/23/2024
    110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDA authorized genericNDA01277002/23/2024
    Labeler - Saptalis Pharmaceuticals, LLC (080145868)
    Registrant - Saptalis Pharmaceuticals, LLC (080145868)