Halodine Nasal Antiseptic Swabstick
Product Images NDC 78371-301

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Halodine Nasal Antiseptic Swabstick (NDC 78371-301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Halodine 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

78371301 12

Packaging label for Halodine Nasal Antiseptic Swabstick containing Povidone-Iodine USP, 2.5%. The label indicates 6 single-use swabsticks, each with 0.5 ml, in 20 packs of 6 swabsticks. The product is marketed by Halodine LLC and highlights a 4-hour formula that helps reduce the risk of infection. The label includes drug facts detailing the active ingredient, uses, warnings, directions, and additional information.*

FDA Label Image

7837130101

Halodine Nasal Antiseptic Swabstick packaging label showing the product name, active ingredient Povidone-Iodine USP 2.5%, and non-sterile solution form. The label indicates 100 single-use swabsticks, 0.5 ml per swabstick, manufactured by Halodine LLC. The label includes directions for use, warnings, and contact information on a predominantly blue and purple background with white text.*

FDA Label Image

7837130102

Packaging label for Halodine Nasal Antiseptic Swabstick containing Povidone-Iodine USP 2.5%. The box indicates 6 single-use swabsticks of 0.5 ml each and highlights a 4-hour formula that helps reduce risk of infection. The labeler is Halodine LLC, and the package shows a white swabstick with blue branding. A Drug Facts panel provides active ingredient, uses, warnings, directions, and other information.*

* 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.