Medichoice Pvp Swab
Product Images NDC 39892-0812

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Medichoice Pvp (NDC 39892-0812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by O&m Halyard, 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

Box3 (Box3)

Label for MediChoice PVP Swabsticks, povidone iodine swabs, with 3 swabs per pack and 25 packs per box. The label indicates reorder number PVPS300B, states it is for professional and hospital use, and highlights sterility is guaranteed if unopened. It notes the product is not made with natural rubber latex and is sterile for single use. Distributed by Owens & Minor.*

FDA Label Image

Label (Label)

Label for MediChoice PVP Swabsticks, a topical swab product available in packs of 3. The label includes storage directions such as protecting from sunlight and water damage. It states the product is sterile, not made with natural rubber latex, for single use only, and distributed by Owens Minor in Virginia. Each case contains 500 packs. The label features barcodes and lot information.*

FDA Label Image

Label4 (Label4)

Drug Facts panel for MediChoice PVP Swabsticks with active ingredient Povidone Iodine USP 10% w/w as an antiseptic. It includes uses for skin preparation before surgery and first aid antiseptic for minor cuts and burns. Contains warnings, directions for use, storage instructions, and a list of inactive ingredients.*

FDA Label Image

Label5 (Label5)

MediChoice PVP Swabsticks 3-pack packaging label showing Povidone Iodine swabsticks for professional and hospital use. The label states sterility guaranteed if unopened, not made with natural rubber latex, sterile, and single use only. The labeler is O&M Halyard, Inc. and the NDC is 39892-0812.*

* 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.