Bacteriostatic Sodium Chloride Injection, Solution
Product Images NDC 0404-9953

3 FDA label images from Henry Schein, Inc. · 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 Sodium Chloride (NDC 0404-9953). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

Image1.jpg (Image1)

Image1.jpg (Image1)
A data table listing products by unit of sale and concentration of Sodium Chloride solution. It details trays of 25 plastic fliptop vials and LifeShield plastic fliptop vials with 0.9% concentration in 10 mL, 20 mL, and 30 mL sizes.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
Label for Bacteriostatic Sodium Chloride injection, USP, multiple dose, 0.9% concentration, 10 mL vial. The label states it is for drug diluent use only, not for inhalation or use in neonates, and requires aseptic technique. Manufactured and packaged by Henry Schein, Inc., with storage instructions at controlled room temperature 68°F to 77°F. Includes NDC 0404-9953-10 and barcode.*
FDA Label Image

Label2.jpg (Label2)

Label2.jpg (Label2)
Label for Bacteriostatic Sodium Chloride 0.9% injection, USP, multiple dose vial. The solution is 30 mL in volume. Includes usage warnings such as not for inhalation or use in neonates, sterile and nonpyrogenic diluent instructions, and storage at controlled room temperature 68°F to 77°F. The label indicates the product is packaged by Henry Schein, Inc., with an NDC of 0404-9953-30. Additional lot, expiration, and barcode information are present but not fully legible.*

* 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.