Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 72572-029

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 72572-029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Chemical Structure (Vancomycin 01)

FDA Label Image

Civica Logo (Vancomycin 02)

FDA Label Image

Principal Display Panel (1 g Vial Label)

Principal Display Panel (1 g Vial Label)
This is a prescription medication labeled for intravenous use. The medication is Vancomycin Hydrochloride for Injection, USP. It is recommended to dilute it with Sterile Water for Injection before use and to refrigerate after dilution. Further dilution is necessary before use. The manufacturer is Civica, Inc., located in Lehi, Utah. For more detailed instructions and precautions, consult the insert provided.*
FDA Label Image

Principal Display Panel (1 g Vial Carton)

Principal Display Panel (1 g Vial Carton)
Description: The text mentions details about Vancomycin Hydrochloride for Injection as a sterile powder that needs further dilution before intravenous use. It describes single-dose fliptop vials containing 10 units and provides information about its usage. The product is identified with NDC code 72572-029-10 and is intended for prescription use only. The text includes additional information about the product's packaging and location of manufacture.*

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