Antiseptic
Product Images NDC 61010-7000

2 FDA label images from Safetec Of America · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Antiseptic (NDC 61010-7000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safetec Of America, 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

Principal Display Panel – Packet Label (Iso01 0003 01)

Principal Display Panel – Packet Label (Iso01 0003 01)
Packaging label for Safetec's Antiseptic I.V. Prep Antiseptic/Barrier Wipe containing a single-use, premoistened towelette. The label states it is for preparation of the skin prior to injection or venipuncture and is manufactured by Safetec of America in Buffalo, NY. The back panel includes Drug Facts detailing isopropyl alcohol 71.5% as the active ingredient and typical usage, warnings, directions, and inactive ingredients.*
FDA Label Image

Principal Display Panel – Box (Iso01 0003 02)

Principal Display Panel – Box (Iso01 0003 02)
Drug Facts panel for Antiseptic I.V. PREP Antiseptic/Barrier Wipe by Safetec. Lists active ingredient as Isopropyl Alcohol 71.5%, purpose as antiseptic, uses for skin preparation before injection or venipuncture, warnings including flammability and external use only, directions for use, and inactive ingredients. Manufacturer information for Safetec of America, Inc. is included. Accompanying product branding panels show product name, labeler, reorder number, and that the package contains 50 single-use premoistened towelettes.*

* 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.