Anusol Hc Suppository
Product Images NDC 65649-411

3 FDA label images from Salix Pharmaceuticals, Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Anusol Hc (NDC 65649-411). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Salix Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Opening Instructions (900177a6 Ffb4 4a0e Aa77 94959a9faaf5 00)

Opening Instructions (900177a6 Ffb4 4a0e Aa77 94959a9faaf5 00)
Instructional diagram showing the steps to remove a suppository from a plastic blister pack. The three-step sequence illustrates pressing down on the blister individual compartment, pushing the suppository through the foil backing, and then removing it for use.*
FDA Label Image

Structural Formula (Anusol Hc 7335 Figure 1 2 17 2011 2 31 54 Pm)

Structural Formula (Anusol Hc 7335 Figure 1 2 17 2011 2 31 54 Pm)
Chemical structure of hydrocortisone acetate, the active ingredient in Anusol HC rectal suppository 25 mg by Salix Pharmaceuticals. The diagram shows the molecular arrangement of atoms including hydroxyl, acetyl, and ketone groups characteristic of hydrocortisone acetate.*
FDA Label Image

Carton

Carton
Packaging label for Anusol-HC 25 mg rectal suppositories, containing Hydrocortisone Acetate in a hydrogenated vegetable oil base. The label indicates a 12 suppository count and is marked Rx only. Manufactured by Salix Pharmaceuticals, Inc. The label includes usage directions stating it is for rectal use only, not oral use, and features the product NDC 65649-411-12 along with a barcode.*

* 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.