Bacteriostatic Water Injection, Solution
Product Images NDC 84502-115

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 Bacteriostatic Water (NDC 84502-115). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fujian Genohope Biotech Ltd., 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

Carton Label For Bacteriostatic Water (Carton Label For Bacteriostatic Water)

Carton Label For Bacteriostatic Water (Carton Label For Bacteriostatic Water)
Box packaging label for Bacteriostatic Water for Injection, USP 1 mL/mL by Fujian Genohope Biotech Ltd. The label includes usage warnings such as "Not for use in neonates" and indicates it contains benzyl alcohol as a preservative. The label also notes the product is for drug diluent use only and specifies routes of administration including intramuscular, intravenous, and subcutaneous injection.*
FDA Label Image

Description For Bacteriostatic Water (Description For Bacteriostatic Water)

Description For Bacteriostatic Water (Description For Bacteriostatic Water)
This text panel describes the description section of Bacteriostatic Water for Injection, USP. It details that the solution is sterile, nonpyrogenic water containing 0.9% benzyl alcohol as a bacteriostatic preservative, supplied in a multiple-dose vial. The product is intended for parenteral use after dilution or dissolution of drugs. The vial is made of neutral borosilicate glass (USP type I) and meets USP powdered glass standards.*
FDA Label Image

Vial_label_bacteriostatic_water (Vial Label Bacteriostatic Water)

Vial_label_bacteriostatic_water (Vial Label Bacteriostatic Water)
Label of Bacteriostatic Water for Injection, USP, 30 mL multiple-dose glass vial. The label notes 0.9% benzyl alcohol added and states it is for drug diluent use only. Directions include using only if clear with intact seal, and cleansing stopper with antiseptic. The label indicates it is prescription-only, not for use in neonates, and includes placeholders for lot number, expiration date, distributor name, address with ZIP code, a company logo, and a barcode.*

* 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.