Hydrocortisone Acetate
Product Images NDC 70795-2412

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocortisone Acetate (NDC 70795-2412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Graxcell Pharmaceutical, 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

Hydrocortisone Acetate 12ct (Hydrocortisone Acetate 12ct)

Packaging label for Hydrocortisone acetate suppositories 25mg by Graxcell Pharmaceutical, LLC. The label indicates a package containing 12 suppositories for rectal administration. Instructions for use and storage conditions are included, along with product and manufacturer information, NDC 70795-2412.*

FDA Label Image

Hydrocortisone Acetate 24ct (Hydrocortisone Acetate 24ct)

Packaging label for Hydrocortisone acetate suppositories 25mg by Graxcell Pharmaceutical, LLC. The label indicates the product contains 24 suppositories and is for rectal administration. The label includes directions for use, storage instructions, and a note on dosage. The NDC number 70795-2412 is shown, along with the labeler and distributor information.*

FDA Label Image

Hydro Structural Formula (Hydro Structural Formula)

Chemical structure diagram of hydrocortisone acetate, showing the molecular arrangement typical of this corticosteroid compound.*

FDA Label Image

Suppo 2 (Suppo 2)

Illustration showing a step-by-step process to open a series of connected plastic ampules or vials, likely for a liquid medication. It depicts fingers pressing down to break the neck of an individual ampule and then removing the top to access the contents. This instructional diagram is related to HYDROCORTISONE ACETATE product use.*

* 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.