Active Ingredient
Hydrocortisone 1.0%
The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Hydrocortisone (NDC 50090-0232). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Hydrocortisone 1.0%
Anti-itch
for the temporary relief of itching associated with minor skin irritations, inflammation and rashes due to:
Other uses of this product should be only under the advice and supervision of a doctor.
If swallowed, get medical help or contact a Poison Control Center immediately.
Adults and children 2 years of age and older
Children under 2 years of age
For external anal itching
You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.
cetyl alcohol, diazolidinyl urea, isopropyl palmitate, mineral oil/lanolin alcohol, polysorbate 40, propylene glycol, propylene glycol monostearate, purified water, sorbic acid, sorbitan monopalmitate, stearyl alcohol, xanthan gum
Product: 50090-0232
NDC: 50090-0232-0 28.4 g in a TUBE
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