Label: HYDROCORTISONE cream

  • NDC Code(s): 73141-622-28, 73141-622-54
  • Packager: A2A Integrated Pharmaceuticals, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 31, 2025

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  • Active ingredient
    Hydrocortisone 1%
  • Purpose
    Anti-Itch
  • Uses
    temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to: eczema - insect bites - poison ivy, oak, or sumac - soaps - detergents - cosmetics - jewelry - seborrheic ...
  • Warnings
    For external use only - Do not use - in the genital area if you have a vaginal discharge. Consult a doctor. for the treatment of diaper rash. Consult a doctor. When using this ...
  • Directions
    for itching of skin irritation, inflammation, and rashes: 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 ...
  • Other information
    store at 20-25°C (68-77°F)
  • Inactive ingredients
    Cetyl alcohol, glycerin, glyceryl stearate SE, mineral oil, PEG-100 stearate, phenoxyethanol, purified water, stearyl alcohol, white petrolatum, xanthan gum
  • Questions or comments?
    Call 1(800)380-6709 - Distributed By: A2A Integrated Pharmaceuticals - Bowling Green, KY 42101
  • Carton Label
    NDC 73141-622-28 - Hydrocortisone Cream 1% Maximum Strength Anti-Itch Cream - NET WT 1 OZ (28g)
  • Jar Label
    NDC 73141-622-54 - Hydrocortisone Cream 1% Maximum Strength Anti-Itch Cream - NET WT 1LB (454g)
  • INGREDIENTS AND APPEARANCE
    Product Information