Borax Pellet
Product Images NDC 76472-3006

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Borax (NDC 76472-3006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sevene Usa, 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

Borax 200ck (Page3 Label Ollois Common)

A partial drug facts panel for Borax 200ck pellets showing inactive ingredient as organic sucrose. The panel includes homeopathic dilution notations (C, K, CK, & X) and distributor contact information for SEVENE USA. It also has illustrated instructions on how to dispense pellets by turning the dispensing tube upside down, twisting the cap, and using the cap to place pellets under the tongue.*

FDA Label Image

Borax 200ck (Label Ollois Borax 200ck Page1)

Label for Borax 200ck homeopathic medicine by SEVENE USA, NDC 76472-3006-1. The product contains approximately 80 pellets (4g) of sublingual pellets with sodium borate. The label indicates it is organic and lactose-free, traditionally used for canker sores. The product is made in France and includes a barcode.*

FDA Label Image

Borax 200ck (Label Ollois Borax 200ck Page2)

Drug Facts panel for Borax 200CK pellets. It lists the active ingredient as Borax 200CK, with uses for canker sores (mouth ulcers). Warnings include stopping use if symptoms worsen or persist beyond 3 days, consulting a doctor if pregnant or breastfeeding, keeping out of children's reach, and seeking medical help in case of overdose. Directions advise dissolving 5 pellets under the tongue three times a day. Additional information includes storage instructions and sealing integrity advice.*

* 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.