Enamelon Paste, Dentifrice
Product Images NDC 48783-520

2 FDA label images from Premier Dental Products Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Enamelon (NDC 48783-520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Premier Dental Products 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

Premier Enamelon Fluoride Toothpaste Mint Breeze 0.75 Oz (21.2 G) (Sample)

Premier Enamelon Fluoride Toothpaste Mint Breeze 0.75 Oz (21.2 G) (Sample)
The packaging label for Enamelon Fluoride Toothpaste paste dentifrice by Premier Dental Products Company. It contains 0.75 oz (21.2 g) with stannous fluoride 0.45% (0.16% w/v fluoride ion) as the active ingredient. The label features product uses for anticavity, antigingivitis, and sensitive teeth, includes directions for use, warnings, inactive ingredients, and distribution information. The design uses blue, white, and red colors with the mint breeze flavor noted.*
FDA Label Image

Premier Enamelon Fluoride Toothpaste Mint Breeze 4.3 Oz (122 G) (Toothpaste)

Premier Enamelon Fluoride Toothpaste Mint Breeze 4.3 Oz (122 G) (Toothpaste)
Packaging label for Enamelon fluoride toothpaste paste, dentifrice, containing stannous fluoride 0.454%. The label shows a 4.3 oz (122 g) tube of mint breeze flavor. The product is marketed by Premier Dental Products Company and highlights use for anticavity, antigingivitis, and sensitive teeth. The label also includes drug facts, active ingredient, warnings, directions, and inactive ingredients.*

* 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.