Label: HYDROCORTISONE ointment

  • NDC Code(s): 51672-2018-2
  • Packager: Sun Pharmaceutical Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 27, 2025

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient
    Hydrocortisone 1%
  • Purpose
    Anti-itch ointment
  • Uses
    temporary relief of itching associated with minor skin irritations and rashes due to - eczema - insect bites - poison ivy, poison oak, or poison ...
  • Warnings
    For external use only - Do not use - in the eyes - by putting this product into the rectum by using fingers or any mechanical device or applicator - Ask a doctor before use if you have - a ...
  • Directions
    Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily - Children under 2 years of age: do not use. consult a doctor - For external anal ...
  • Other information
    To open: unscrew cap, pull tab to remove foil seal, and screw cap back onto tube - store at room temperature - see carton or tube crimp for lot number and expiration date
  • Inactive ingredients
    Fractionated Coconut Oil, Methylparaben, Propylparaben, White Petrolatum
  • Questions?
    Call 1-866-923-4914
  • SPL UNCLASSIFIED SECTION
    Distributed by: Taro Pharmaceuticals - U.S.A., Inc. Hawthorne, NY 10532
  • PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton
    Itch and Rash Relief - MAXIMUM STRENGTH - Hydrocortisone 1% Ointment - Antipruritic (Anti-Itch) NET WT 1 oz (28.4 g)
  • INGREDIENTS AND APPEARANCE
    Product Information