Neutrarinse 2% Neutral Sodium Floride Oral Rinse White Grape
Product Images NDC 61508-0527

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Neutrarinse 2% Neutral Sodium Floride Oral Rinse White Grape (NDC 61508-0527). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Germiphene Corporation, 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

White Grape (Nrgr 2)

Neutrarinse 2% Neutral Sodium Fluoride Oral Rinse in White Grape flavor is displayed on this product label. It contains 2 liters (67.6 fl oz) of solution with 2.0% neutral sodium fluoride and xylitol. The label includes usage instructions, warnings, and manufacturer information from Germiphene Corporation, Brantford, Ontario, Canada. The label is bilingual in English and French.*

FDA Label Image

Refreshmint (Nrmt 2)

Label for Neutrarinse 2% Neutral Sodium Fluoride Oral Rinse, a 2-liter oral rinse solution by Germiphene Corporation. The label includes bilingual text in English and French, indicating the active ingredient as 2.0% neutral sodium fluoride, with added xylitol and a RefreshMint flavor. Instructions for topical use to prevent dental caries, warnings, and manufacturer information are also present. The product is made in Canada.*

FDA Label Image

Raspberry Splash (Nrvb 2)

Neutrarinse 2% Neutral Sodium Fluoride Oral Rinse Raspberry Splash 2-liter bottle label. The label states it contains 2.0% neutral sodium fluoride with xylitol, is manufactured by Germiphene Corporation in Canada, and includes bilingual text in English and French with directions, warnings, and 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.