Active Ingredient
Hydrocortisone 1%
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Hydrocortisone (NDC 11673-392). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Hydrocortisone 1%
Anti-itch
For external use only
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
aloe powder, cetearyl alcohol/sodium lauryl sulfate/sodium cetearyl sulfate, citric acid, glycerin, glyceryl monostearate, methylparaben, mineral oil, paraffin wax, propylparaben, purified water, sodium lauryl sulfate, stearyl alcohol
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Distributed by Target Corporation
Minneapolis, MN 55403
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