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)

This is a description of a medication product called Hydrocortisone acetate suppositories, containing 25mg of the active ingredient. Each suppository is designed for rectal administration and consists of hydrocortisone acetate and hydrogenated vegetable oil. The packaging includes 12 suppositories, and the product is available only through a prescription (Rx only). It is recommended to store the product at a controlled temperature of 20°C (68°F) and not to use it if the package is broken or tampered with. The text also includes several codes such as NDC 70705-24121 and 31139 au0S|1020IpAH, as well as a manufacturer's name, i.e., GRAXCELL PHARMACEUTICAL, LLC.*

FDA Label Image

Hydrocortisone Acetate 24ct (Hydrocortisone Acetate 24ct)

Hydrocortisone acetate suppositories 25mg are a rectal treatment used for reduced pain and inflammation. The package includes a complete set of dosing and administration instructions. The suppository is gently placed into the rectum and should not be overhandled or subjected to heat. The product should be stored at a controlled temperature. There are 24 suppositories per package.*

FDA Label Image

Hydro Structural Formula (Hydro Structural Formula)

FDA Label Image

Suppo 2 (Suppo 2)

* 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.