Pcxx Creme De Menthe Apf G Gel
Product Images NDC 62007-806

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 Creme De Menthe Apf G (NDC 62007-806). 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.

Product Images & Figures Index

FDA Label Image

42f1377f 369e F530 E063 6394a90ab892

42f1377f 369e F530 E063 6394a90ab892
Drug information panel for PCXX CREME DE MENTHE APF G Sodium Fluoride topical gel 2.72% concentration. Contains directions for professional use anticavity treatment, listing steps for application and precautions. Lists medicinal ingredient as sodium fluoride and non-medicinal ingredients including monosodium phosphate, flavorings, and colorants. Includes warnings for use in adults and children over age 6, and contact info for Ross Healthcare Inc. Package size noted as 475 ml / 16 fl oz.*
FDA Label Image

Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
PCXX Neutral 2.0% Sodium Fluoride Topical Gel packaging label featuring the PCXX logo and Bazooka Bubble Gum graphic. The label provides directions, warnings, and ingredients, listing sodium fluoride as the active ingredient and mentioning medicinal ingredients such as flavor and other components. It includes usage and storage instructions, cautions to keep out of reach of children, and regulatory information, all on a white background.*

* 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.