Ludent
Product Images NDC 44946-1017

3 FDA label images from Sancilio & Company 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 Ludent (NDC 44946-1017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sancilio & Company 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

Principal Display Panel (0.25 mg Tablet Label)

Principal Display Panel (0.25 mg Tablet Label)
Ludent Fluoride Chews chewable fluoride tablets with 0.25 mg active fluoride per tablet, containing 120 tablets per container. The label states the product is sugar and dye free, Rx only, and made in the U.S.A. by Sancilio & Company, Inc. The label includes usage directions, storage information, a barcode, lot number, and expiration date fields.*
FDA Label Image

Principal Display Panel (0.5 mg Tablet Label)

Principal Display Panel (0.5 mg Tablet Label)
Ludent Fluoride Chews chewable fluoride tablets, 0.5 mg strength, containing 120 tablets per package. The label shows active ingredient details, usage instructions, and cautions, specifying the product is Rx only and made by Sancilio & Company Inc in the USA. The NDC code and barcode are also visible.*
FDA Label Image

Principal Display Panel (1.0 mg Tablet Label)

Principal Display Panel (1.0 mg Tablet Label)
Ludent Fluoride Chews chewable fluoride tablets, 1.0 mg strength, with 120 tablets per bottle. Manufactured by Sancilio & Company Inc. Label notes sugar and dye free, Rx only, and fluoride source equivalent to 2.2 mg sodium fluoride per tablet. Package includes usage and ingredient details.*

* 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.