Procort Cream
Product Images NDC 50967-357

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Procort (NDC 50967-357). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Womens Choice Pharmaceuticals Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Procortpi2

This text panel provides patient information, warnings, dosage and administration instructions, adverse reactions, overdose information, and storage conditions for PROCORT cream containing 1.85% hydrocortisone acetate and 1.15% pramoxine HCl. It includes specific directions for rectal administration, laboratory test considerations, and notes on use in pediatric and pregnant patients.*

FDA Label Image

Procort Pi

This image displays detailed prescribing information for PROCORT cream, a topical medication with active ingredients hydrocortisone acetate 1.85% and pramoxine hydrochloride 1.15%. The text covers clinical pharmacology, pharmacokinetics, indications, contraindications, and precautions, including the anti-inflammatory and anesthetic properties, systemic absorption risks, and recommended patient monitoring during use.*

FDA Label Image

Updated2018

The image shows a flattened packaging label for PROCORT cream containing 1.85% hydrocortisone acetate and 1.15% pramoxine HCl. The label features branding with the PROCORT name, claims of fast-acting dual action relief, and instructions indicating it is a topical prescription cream. The label displays dosage form as cream, the labeler as Womens Choice Pharmaceuticals LLC, and includes barcodes, NDC 50967-357-40, and usage directions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.