Pcxx Remin 0.4
Product Images NDC 62007-041

2 FDA label images from Ross Healthcare Inc. · 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 Pcxx Remin 0.4 (NDC 62007-041). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ross Healthcare 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

Front Panel Rmg (Front Panel Rmg)

Front Panel Rmg (Front Panel Rmg)
The label for PCXX REMIN 0.4 Remin Gel features the brand name and indicates it is a sodium fluoride topical gel with an ice mint flavor. Instructions for use include not swallowing, using after brushing, brushing thoroughly before application, and not eating or drinking for 30 minutes after use. The label lists the active ingredient as sodium fluoride and other medicinal ingredients. The product is labeled by Ross Healthcare Inc.*
FDA Label Image

Secondary Panel Rmn (Secondary Panel Rmn)

Secondary Panel Rmn (Secondary Panel Rmn)
This is a drug facts panel for PCXX REMIN 0.4 by Ross Healthcare Inc. It includes directions for use such as not swallowing, using after brushing teeth, and brushing thoroughly for one minute before expectorating. The medicinal ingredient listed is 0.4% sodium fluoride along with non-medicinal ingredients like sodium metabisulfite and potassium sorbate. The label also references the product NDC 62007-041-02 and includes a lot number and expiration date.*

* 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.