Pvp-i Prep Pads Foil-foil Swab
Product Images NDC 65517-0034

3 FDA label images from Dukal Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pvp-i Prep Pads Foil-foil (NDC 65517-0034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dukal 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.

Product Images & Figures Index

FDA Label Image

Dukal Pvp Preppad 889 Item China

Dukal Pvp Preppad 889 Item China
Drug Facts panel for Povidone-Iodine Pad by Dukal Corporation, NDC 65517-0034-2. Includes active ingredient Povidone Iodine USP 10% as antiseptic, instructions for use prior to surgery, warnings about external use, allergy, and keeping out of reach of children. Also lists inactive ingredients and storage information.*
FDA Label Image

Principal Display Panel (PVP-I Prep Pads Foil Pouch Label)

Principal Display Panel (PVP-I Prep Pads Foil Pouch Label)
Label for Povidone-iodine Pad antiseptic swab, sterile, for professional and hospital use only. Manufactured by Dukal Corporation, Ronkonkoma, NY. Package indicates one pad per pouch, with NDC 65517-0034-1. Includes warnings, directions, active ingredient Povidone Iodine USP 10%, and inactive ingredients listed. Not made with natural rubber latex.*
FDA Label Image

Principal Display Panel (PVP-I Prep Pads Foil 865-8000 Case Label)

Principal Display Panel (PVP-I Prep Pads Foil 865-8000 Case Label)
PVP-I Prep Pads foil-foil packaging label for Povidone-iodine sterile swabs, labeled with 8000 pads per case and 1 pack per case. The label features the Dukal LLC logo, indicates professional and hospital use, and states the product is not made with natural rubber latex. Manufactured by Dukal Corporation with product NDC 65517-0034.*

* 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.