Super Vanilla Prescription
Product Images NDC 83729-100

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Super Vanilla Prescription (NDC 83729-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Supermouth, Llc., 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

Vanilla Box (Vanilla Box)

Packaging label for Super Vanilla Prescription SuperMouth anticavity toothpaste by SuperMouth, LLC. Features 1.1% sodium fluoride (5000 ppm) strength with prescription fluoride and hydroxamin ingredients. The label highlights professional use only, anticavity properties, and a Super Vanilla flavor. The product net content is 1 tube, 3.4 oz (96g). Additional information includes directions, active ingredients, warnings, and a barcode.*

FDA Label Image

Vanilla Tube (Vanilla Tube)

Packaging label for Super Vanilla Prescription anticavity toothpaste with 1.1% sodium fluoride strength. The label highlights the product's prescription fluoride and hydroxamin content, branded under SuperMouth, LLC. The tube contains 3.4 ounces (96 grams). The label includes usage warnings, directions, inactive ingredients, and distributor information from SuperMouth in San Diego, California.*

* 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.