Eversmile Ipr Glide Gel
Product Images NDC 72655-400

View Photos of 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 Eversmile Ipr Glide (NDC 72655-400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Everbrands, Inc. Dba Everpure, 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

Ipr Glide 1 mL Syringe (Ipr Glide 1 mL Syringe)

Ipr Glide 1 mL Syringe (Ipr Glide 1 mL Syringe)
Eversmile IPR Glide 2.7% Neutral Sodium Fluoride Gel in a 1 mL single-use dispenser syringe. The transparent plastic syringe is labeled with concentration and volume, intended for dental topical application. Labeler is Everbrands, Inc. dba Everpure, Inc.*
FDA Label Image

Ipr Glide 4 mL Syringe (Ipr Glide 4 mL Syringe)

Ipr Glide 4 mL Syringe (Ipr Glide 4 mL Syringe)
Eversmile IPR Glide (2.7% Neutral Sodium Fluoride) dental gel in a 4 mL (0.134 oz) syringe dispenser. The syringe is clear with black text on the label and a black plunger. Labeler is Everbrands, Inc. dba Everpure, Inc.*
FDA Label Image

Ipr Glide 4 mL Box (Ipr Glide 4ml Box)

Ipr Glide 4 mL Box (Ipr Glide 4ml Box)
The packaging label for Eversmile IPR Glide 2.7% Sodium Fluoride Gel shows a 4 mL dental gel designed to lubricate and strengthen enamel. The label includes usage instructions for interproximal reduction and post-treatment fluoride application. It lists active and inactive ingredients, manufacturer Everbrands, Inc., and a fresh mint flavor. The product is prescription-only, with directions for use and precautions noted.*

* 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.