Active Ingredient
Hydrocortisone USP 1%
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health for the product Hydrocortisone (NDC 70000-0485). 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, if pregnant or breast-feeding,, do not use, 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 USP 1%
Antipruritic (Anti-Itch)
For external use only
ask a health professional before use.
If swallowed, get medical help or contact a Poison Control Center (1-888-222-1222) right away.
Store at room temperature
Cetostearyl Alcohol, Glyceryl Palmitostearate, Kathon, Petrolatum, Propylene Glycol, Stearic Acid, Tea Leaf, Water
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* Please review the disclaimer below.