Sterile Water Injection
Product Images NDC 51662-1265

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

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sterile Water (NDC 51662-1265). 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

Serialized Label (Serialized 51662 1265 1 Sterile Water 50)

Serialized Label (Serialized 51662 1265 1 Sterile Water 50)
50 mL vial of Sterile Water for Injection, USP, single-dose. The label states it is for drug diluent use and is manufactured for Hospira, Inc., Lake Forest, IL. A barcode and distributor information for HF Acquisition Co., LLC, Mukilteo, WA are also visible on the label.*
FDA Label Image

Vial (Vial Label)

Vial (Vial Label)
Packaging label for Sterile Water for Injection, USP in a 50 mL single-dose vial. The label states that the solution is for drug diluent use, sterile, nonpyrogenic, and contains no antimicrobial or other added substances. The label shows the manufacturer as Hospira, Inc., Lake Forest, IL, with an NDC code 0409-4887-24.*
FDA Label Image

How Supplied (How Supplied 1)

How Supplied (How Supplied 1)
A data table listing various unit of sale options and total content volumes for sterile water injections. It includes NDCs for trays or cases of glass or plastic fliptop vials, with volumes ranging from 1 mL to 100 mL per vial.*

* 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.