Xesso Rear Comfort Glide Gel
Product Images NDC 81777-104

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Xesso Rear Comfort Glide (NDC 81777-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Premium Natural Cosmetics 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

Inactives (Inactive Ingredients)

A text panel listing inactive ingredients in the product, including Carboxymethylcellulose Sodium, Diazolidinyl urea, Glycerin, Isopentyldiol, Methylparaben, Propylparaben, and Water.*

FDA Label Image

Warning (Warning)

A warnings panel for Xesso Rear Comfort Glide (Lidocaine) gel stating it is for external use only and should not be used with a mechanical device. It warns about possible allergic reactions, advises discontinuing use and consulting a doctor if symptoms worsen, instructs not to exceed the daily dose, avoid applying on cracked or broken skin, and to stop use and seek medical help if bleeding occurs.*

FDA Label Image

Label Proof (Xesso Rear Comfort Lube 2percent Lidocaine)

Label for Xesso Rear Comfort Glide gel, containing 2% lidocaine, designed for rectal use. The label features a black background with white and light blue text. It highlights features like 'slippery & mild numbing,' 'thick, water-based formula,' 'PEG-Free & Oil-Free,' and displays the volume as 8.3 fl. oz. (245 mL). The label includes a Drug Facts panel with active ingredient, warnings, directions, and inactive ingredients, along with manufacturer information for Premium Natural Cosmetics Inc. A barcode and symbols indicating product attributes are also present.*

* 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.