Hydrocortisone Acetate Suppository
Product Images NDC 82568-0150

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrocortisone Acetate (NDC 82568-0150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aarna Usa Inc., 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

2 (Hydro 25mg 12ct)

2 (Hydro 25mg 12ct)
The text provides detailed instructions for the use of Hydrocortisone Acetate Suppositories for rectal administration. The suppositories contain 25 mg of hydrocortisone acetate in a hydrogenated vegetable oil base. It advises on how to properly handle and insert the suppository and includes warnings to store the product correctly, avoid contact with eyes, and keep it out of reach of children. Additionally, it mentions the importance of consulting the package insert for complete prescribing information before use. There is a caution for pharmacists regarding the product not being FDA tested for therapeutic equivalence and the need to comply with state and federal statutes when prescribing.*
FDA Label Image

3 (Hydro 25mg 24ct)

3 (Hydro 25mg 24ct)
This is a description of Hydrocortisone Acetate Suppositories for rectal administration. Each suppository contains 25 mg of hydrocortisone acetate in a hydrogenated vegetable oil base. The directions instruct to insert one suppository rectally as directed for dosage and administration. It is advised to avoid excessive handling as the suppository is designed to melt at body temperature. The product should be stored at 20°-25°C and away from heat or freezing conditions. In case of accidental ingestion, seek professional assistance or contact Poison Control immediately. This product has not been FDA tested for therapeutic equivalence; therefore, any prescription recommendation should be based on professional knowledge. The packaging includes 24 unit doses of suppositories. Manufacturers are listed as AarnaUSA Inc from Leand, NC. The NDC code for this product is 82568-0150-2.*
FDA Label Image

4 (Hydro 30mg 12ct)

4 (Hydro 30mg 12ct)
This text contains information about Hydrocortisone Acetate Suppositories for rectal administration. It provides details on how to use the suppositories, including directions for insertion and storage conditions. The dosage and administration instructions are also included. The text mentions the NDC (National Drug Code) for the product. It is important to consult the enclosed package for complete prescribing information before use. The product is not an Orange Book rated product, and any prescriptions using it should adhere to state and federal statutes.*
FDA Label Image

Chemical Structure (Hydrocortisone 01)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.