Bacteriostatic Water Injection, Solution
Product Images NDC 51662-1473

9 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Bacteriostatic Water (NDC 51662-1473). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A table listing units of sale for products with different benzyl alcohol preservative concentrations. It includes NDC numbers, package configurations showing trays of multiple-dose fliptop vials in plastic or glass, and benzyl alcohol concentrations of 9 mg/mL and 11 mg/mL respectively.*
FDA Label Image

Serialized Vial Labeling (Seerialized Labeling)

Serialized Vial Labeling (Seerialized Labeling)
BACTERIOSTATIC WATER injection solution in a clear vial with a purple cap and label from HF Acquisition Co LLC, DBA HealthFirst. The label shows 30 mL multiple-dose vial, marked "not for use in neonates" and includes a QR code with lot and expiration information.*
FDA Label Image

Spl (Spl Unclassified)

Spl (Spl Unclassified)
A warning panel stating: 'WARNING: NOT FOR USE IN NEONATES.' This label highlights a usage caution for Bacteriostatic Water injection, solution.*
FDA Label Image

Principal Display Panel (VIAL LABEL OPTION 1)

Principal Display Panel (VIAL LABEL OPTION 1)
The label for BACTERIOSTATIC WATER injection, USP, 30 mL multiple-dose vial, labeled for use as a drug diluent only. It includes warnings such as 'NOT FOR USE IN NEONATES' and states the solution contains 0.9% benzyl alcohol. Manufactured by Hospira, Inc., Lake Forest, IL, with NDC 0409-3977-01.*
FDA Label Image

Principal Display Panel (VIAL LABEL OPTION 2)

Principal Display Panel (VIAL LABEL OPTION 2)
Label for BACTERIOSTATIC WATER injection, USP, 30 mL multiple-dose vial. Indicates 0.9% benzyl alcohol added and states it is sterile and nonpyrogenic. Label includes warnings for use only if seal is intact and not for use in neonates. Distributed by Hospira, Inc., Lake Forest, IL.*
FDA Label Image

Principal Display Panel (VIAL LABEL OPTION 3)

Principal Display Panel (VIAL LABEL OPTION 3)
Label for Bacteriostatic Water injection, USP, 30 mL multiple-dose vial. Contains 0.9% benzyl alcohol as a bacteriostatic agent. Label indicates use as drug diluent only and not for use in neonates. Manufactured for Hospira, Inc., Lake Forest, IL, by a facility in India. Includes NDC 0409-3977-01 and instructions to cleanse stopper with antiseptic before use. Features an area designated for a 2D barcode with human-readable GTIN, serial number, lot, and expiry information.*
FDA Label Image

Principal Display Panel (VIAL LABEL OPTION 4)

Principal Display Panel (VIAL LABEL OPTION 4)
Label for Bacteriostatic Water for Injection, USP, 30 mL multiple-dose vial. The label states it is not for use in neonates and contains 0.9% benzyl alcohol added. It is sterile, nonpyrogenic, and intended for use as a drug diluent only. The product is distributed by Hospira, Inc., Lake Forest, IL.*
FDA Label Image

Principal Display Panel (VIAL LABEL OPTION 5)

Principal Display Panel (VIAL LABEL OPTION 5)
Label of BACTERIOSTATIC WATER for Injection, USP, 30 mL multiple-dose vial. The label indicates it is for drug diluent use only, contains 0.9% benzyl alcohol as a preservative, is sterile and nonpyrogenic, and not for use in neonates. Manufactured by Hospira, Inc., Lake Forest, IL, with NDC 0409-3977-01.*

* 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.