Hydrocortisone
FDA Label NDC 63941-229

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Valu Merchandisers, Co. for the product Hydrocortisone (NDC 63941-229). 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, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Purpose

Anti-itch

Warnings

For external use only

Inactive Ingredient

aloe barbadensis leaf juice, aluminum sulfate, beeswax, calcium acetate, cetyl alcohol, dextrin, glycerin, maltodextrin, methylparaben, mineral oil, petrolatum, propylparaben, sodium cetearyl sulfate, sodium lauryl sulfate, water

Package Label

Best Choice Hydrocortisone with Aloe

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