Dx1 Oragenomic Medicated Dna Collection Screen
Product Images NDC 70529-441

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dx1 Oragenomic Medicated Dna Collection Screen (NDC 70529-441). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by It3 Medical 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

Comp1 (Compdx1)

Comp1 (Compdx1)
This is a package containing Benzalkonium Chloride Towelette, a Firstaid antiseptic designed to help prevent skin infection. The product is sterile, latex-free, and can be used for minor cuts, burns, and bruises. It is a single-use only item, recommended to store at room temperature, and manufactured by PSS World Medical. The package contains 1 towelette and the reorder number is 269. The product should not be used in the eyes or applied over large areas of the body for more extended periods than one week without consulting a doctor. If the product gets swallowed, contact a Poison Control Center to receive medical help. The inactive ingredients of the product include purified water and sodium bicarbonate.*
FDA Label Image

Dx1 System (Dx1)

Dx1 System (Dx1)
This is a description of a product called "OraGenomic Medicated DNA Collection Screen" which includes PGX screening using an oral swab with lidocaine hydrochloride solution. The product is identified with the National Drug Code (NDC) number 70529-441-01.*
FDA Label Image

Comp2 (Lemonswab)

Comp2 (Lemonswab)
This is a description of an oral swab with lemon glycerin. Each packet contains three swabs, and there are 25 packets in a box. It is distributed by Cardinal Health and not made with natural rubber latex. The product is for single use only and should be kept dry and out of direct sunlight. The directions for use indicate that the swab should be moistened before application. There is also a note that the product should be used under supervision and that the Cardinal Health logo is trademarked. The inactive ingredients include berzote. The part number for this product is OC-SWBLG(C)1, and the NDC number is 63517-160-01.*
FDA Label Image

Struct-1 (Structure 1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.