Vancomycin Hydrochloride
Product Images NDC 72572-803

View Photos of 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 Vancomycin Hydrochloride (NDC 72572-803). 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)

Chemical Structure (Vancomycin 01)
Chemical structure of Vancomycin Hydrochloride showing its detailed molecular formula with atoms and bonds.*
FDA Label Image

Principal Display Panel (5 gram Bottle Carton)

Principal Display Panel (5 gram Bottle Carton)
Packaging label for Vancomycin Hydrochloride for Injection, USP, 5 grams per pharmacy bulk package. The label indicates the product is a sterile lyophilized powder in a single bottle. It is for intravenous use after dilution and must be further diluted before use. The label includes warnings that the bulk package is not for direct infusion and instructions to discard the bottle no later than 4 hours after initial entry. Labeler is Civica, Inc.*
FDA Label Image

Principal Display Panel (10 gram Bottle Carton)

Principal Display Panel (10 gram Bottle Carton)
Packaging label for Vancomycin Hydrochloride for Injection, USP, 10 grams, pharmacy bulk package by Civica, Inc. The label states it is sterile lyophilized powder for intravenous use after dilution, with warnings that it is not for direct infusion and must be further diluted before use. Preservative free, each bottle contains 10 g vancomycin equivalent. The label includes storage, preparation instructions, and notes on usage and disposal.*

* 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.