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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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Active ingredient
Hydrocortisone 1%
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Purpose
Anti-Itch
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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 ...
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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 ...
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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 ...
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Other information
store at 20-25°C (68-77°F)
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Inactive ingredients
Cetyl alcohol, glycerin, glyceryl stearate SE, mineral oil, PEG-100 stearate, phenoxyethanol, purified water, stearyl alcohol, white petrolatum, xanthan gum
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Questions or comments?
Call 1(800)380-6709 - Distributed By: A2A Integrated Pharmaceuticals - Bowling Green, KY 42101
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Carton Label
NDC 73141-622-28 - Hydrocortisone Cream 1% Maximum Strength Anti-Itch Cream - NET WT 1 OZ (28g)
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Jar Label
NDC 73141-622-54 - Hydrocortisone Cream 1% Maximum Strength Anti-Itch Cream - NET WT 1LB (454g)
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INGREDIENTS AND APPEARANCEProduct Information