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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Aldermed Inc. for the product Hydrocortisone (NDC 87236-004). 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 other, active ingredient, purpose, uses, warnings, do not use, ask a doctor before use if you are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Hydrocortisone USP 1%
Antipruritic (Anti-itch)
For external use only
using any other hydrocortisone product
If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
Cetostearyl Alcohol, Glyceryl Monostearate SE, Kathon CG, Propylene Glycol, Purified Water, Stearic Acid, Trolamine, White Petrolatum
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