Anorectal Hemorrhoidal Cream With Lidocaine 5%
Product Images NDC 55629-019

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Anorectal Hemorrhoidal Cream With Lidocaine 5% (NDC 55629-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by One2zee Limited Liability Company, 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

4oz Carton (4oz Carton)

Anorectal Hemorrhoidal Cream with Lidocaine 5% packaging label from Health One. The label highlights a 5% lidocaine active ingredient concentration and a 4 oz value size. It features a purple and orange color scheme with child-resistant packaging instructions, drug facts, and usage directions. The product is distributed by ONE2ZEE LIMITED LIABILITY COMPANY.*

FDA Label Image

4oz Tube (4oz Tube)

Packaging label for Anorectal Hemorrhoidal Cream with Lidocaine 5%, a 4 oz (113 g) cream by ONE2ZEE LIMITED LIABILITY COMPANY. The label highlights 5% lidocaine as the active ingredient and displays product size prominently. The label includes drug facts, usage directions, warnings, inactive ingredients, storage information, and a contact number for questions.*

FDA Label Image

5oz Jar (5oz Jar)

Drug Facts panel for Anorectal Hemorrhoidal Cream with Lidocaine 5% detailing active ingredient lidocaine, purpose as anorectal cream, uses for pain relief associated with hemorrhoids, warnings for external use only, directions advising use up to six times daily, inactive ingredients list, storage instructions, and contact information for questions. The panel emphasizes child-resistant packaging and non-prescription status.*

* 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.