Bacteriostatic Water Injection, Solution
Product Images NDC 0409-3977

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 Bacteriostatic Water (NDC 0409-3977). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Hospira Logo (Bacteriostatic 01)

FDA Label Image

Principal Display Panel (30 mL Vial Label)

Principal Display Panel (30 mL Vial Label)
This is a description of a 30 mL multiple-dose medication container with NDC 0409-3977-01. The medication is for drug dilution only and contains 0.9% benzyl alcohol. It is sterile and nonpyrogenic, and the container must only be used if it is clear and the seal is intact and undamaged. The stopper must be cleansed with an antiseptic before use. The medication is not suitable for use in neonates and is distributed by Hospira, Inc. The lot number and expiration date are also mentioned.*
FDA Label Image

Plate Ndc 0409-3977-03 (Bacteriostatic 03)

FDA Label Image

Bacteriostatic 04

Bacteriostatic 04
This is a description for a multiple-dose glass vial that comes in a size of 20 mL. It has NDC code 0409-1093-14 and should be used as a drug diluent only. The vial is sterile, non-pyrogenic and bacteriostatic. It should be used orally if the seal is undamaged and the solution inside is clear. Before use, the stopper should be cleaned using an antiseptic. The vial contains 1.1% benzyl alcohol added and has a lot number and expiration date mentioned. It is not suitable for use in neonates.*
FDA Label Image

Bacteriostatic 05

Bacteriostatic 05
This is a warning about the use of BACTERIOSTATIC WATER FOR INJECTION, USP, which contains 1.1% of benzyl alcohol added as a preservative. The text adds that it must not be used in neonates, as it is indicated only for drug diluent use. It also shows the NDC number and a code for batch identification. The rest of the text seems to be a mix of random characters and symbols, therefore it is not possible to provide further useful information.*

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