Ionite Apf Gel
Product Images NDC 53045-201

3 FDA label images from Dharma Research, 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 Ionite Apf (NDC 53045-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dharma Research, 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

20200415 201 08 Revb

20200415 201 08 Revb
Label for Ionite APF Thixotropic Gel, a dental oral prescription gel containing acidulated phosphate fluoride with 1.23% fluoride ion. The label states it is gluten-free and offers 1 or 4 minute treatment options. Packaging volume is 8.5 fl. oz. (250 ml), manufactured by Dharma Research, Inc., made in USA. The drug facts panel includes active ingredient, warnings, directions, storage, and inactive ingredients details.*
FDA Label Image

20200415 201 17 Revb

20200415 201 17 Revb
Label for Ionite APF Thixotropic Gel, a dental oral gel containing 1.23% fluoride ion. Cherry Tart flavor with Xylitol & Vitamin E, gluten free, available in a 17 fl. oz. (500 ml) bottle. Manufactured by Dharma Research, Inc. The label includes drug facts, warnings, directions, other information, and inactive ingredients.*
FDA Label Image

20200415 201 38 Revb

20200415 201 38 Revb
Label for Ionite APF Thixotropic Gel, a dental oral gel containing acidulated phosphate fluoride with xylitol and vitamin E. The label indicates a fluoride ion concentration of 1.23%, cherry tart flavor, gluten free, and a 1-gallon (3.8L) size. It is manufactured by Dharma Research, Inc. and marked for professional dental use with treatment times of 1 or 4 minutes.*

* 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.