Sterile Water Injection, Solution
Product Images NDC 0143-9339

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sterile Water (NDC 0143-9339). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Sterile Water For Injection, Usp Inner Bag (Sterile Water For Injection Usp 1)

Sterile Water For Injection, Usp Inner Bag (Sterile Water For Injection Usp 1)
This is a 1000 mL single-dose container of sterile water for injection, USP labeled for drug diluent use only. It has a pH of 5.5 and contains no added antimicrobial or other substances. The container must be administered intravenously after being made approximately isotonic with a suitable solute, and any additives should be compatible and added using aseptic technique. The solution should be mixed thoroughly and not stored. The inner bag should be inspected for leaks and discarded if found, and the product should not be used in series connections. The unit should be stored in a moisture barrier wrapper at 20° to 25°C (68 to 77°F) until ready to use. The manufacturer is HIKMA FARMACEUTICA (PORTUGAL), S.A., and the distributor is Hikma Pharmaceuticals USA Inc. Dosage should be determined by a physician, and cautions apply. Contact the pharmacist if necessary. For more information, the package insert should be consulted, and a product information phone line is available.*
FDA Label Image

Sterile Water For Injection, Usp Overwrap (Sterile Water For Injection Usp 2)

Sterile Water For Injection, Usp Overwrap (Sterile Water For Injection Usp 2)
This is a 1000mL single dose container of Sterile Water for Injection, USP with instructions for use as a drug diluent only. It is a sterile, nonpyrogenic container for intravenous administration only after rendering approximately isotonic with a suitable solute. Additives may be incompatible. The inner bag inside the overwrap maintains product sterility. To open the package, it says to tear at the notch. The solution should not be used unless it is clear. The package must be stored in a moisture barrier overwrap at 20° to 25°C until ready to use. Do not store or use if overwrap has been previously opened or damaged. The manufacturer is HIKMA FARMAGEUTICA (PORTUGAL), SA and it is distributed by Hikma Pharmaceuticals USA Inc. This container is for Rx use only and has a National Drug Code of 0143-9339-01.*

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