Nusurgepak Surgical Prep/carepak
Product Images NDC 70859-057

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nusurgepak Surgical Prep/carepak (NDC 70859-057). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals 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

Pdp (Dimethicone)

Pdp (Dimethicone)
The text is not readable.*
FDA Label Image

Dyna-hex 4 Principal Display Panel (Dyna Hex 8)

Dyna-hex 4 Principal Display Panel (Dyna Hex 8)
This is a product description for DYNA-HEX 4, an antiseptic solution containing 4% Chlorhexidine Gluconate, distributed by Xetrium Laboratories. The solution is recommended for a variety of external use, including surgical hand scrub, healthcare personnel handwash, patient preoperative skin preparation, skin wound, and general skin cleansing. It comes with a list of warnings, including not to be used by people who are allergic to Chlorhexidine Gluconate or any other ingredients. It also provides usage instructions and a list of inactive ingredients.*
FDA Label Image

Pdp (Nusurgepak Surgical Prep Carepak)

Pdp (Nusurgepak Surgical Prep Carepak)
This appears to be a collection of product names and codes for various medical supplies such as Ghlorhexidine Gluconate, Mupirocin Ointment, Dimethicone, and silicone tape, along with a description for a Surgical Prep/Care Package called NuSurgePak. No further information is provided.*
FDA Label Image

Ointment-tube (Ointment Tube)

Ointment-tube (Ointment Tube)
Mupirocin is a medication for dermatologic use only, indicated to be applied three times a day to the affected area. Each gram of the ointment has 20mg of the active ingredient, Mupirocin USP, in a polyethylene glycol NF base. Re-evaluation is necessary if there is no clinical response within 3 to 5 days. Glenmark Pharmaceuticals manufacture the ointment and it should be stored at 20°to 25°C (68° to 77°F). The package contains prescribing information with instructions and Glenmark Pharmaceutical's contact information for any questions.*
FDA Label Image

Structure (Structure)

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