Sodium Chloride
Product Images NDC 0409-1918

16 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0409-1918). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Hospira Logo (Sodiumchloride 01)

FDA Label Image

Sodiumchloride 01a

FDA Label Image

Principal Display Panel (10 mL Vial Label)

Principal Display Panel (10 mL Vial Label)
Label of 0.9% Sodium Chloride Injection, USP, 10 mL single-dose vial. The label indicates preservative-free sterile solution with 9 mg sodium chloride per mL, distributed by Hospira, Inc. It includes notation for lot and expiration dates and states use as a sterile diluent.*
FDA Label Image

Principal Display Panel (10 mL Vial Tray)

Principal Display Panel (10 mL Vial Tray)
Label for Sodium Chloride 0.9% Injection, USP sterile diluent, 10 mL single-dose vial packaging. The label includes the NDC 0409-4888-10 and states the product is distributed by Hospira, Inc. It also shows dosage instructions and storage conditions. The label features the Hospira logo and a barcode.*
FDA Label Image

Principal Display Panel (10 mL Vial Label)

Principal Display Panel (10 mL Vial Label)
Label for Sodium Chloride Injection, USP 0.9% 20 mL single-dose vial by Hospira, Inc. The label states it is preservative-free, sterile, and nonpyrogenic, used as a sterile diluent. It lists sodium chloride 9 mg per mL and notes possible pH adjustments with HCl and/or NaOH. Includes NDC 0409-4888-03 and distributor information in Lake Forest, IL.*
FDA Label Image

Principal Display Panel (10 mL Vial Tray)

Principal Display Panel (10 mL Vial Tray)
Label for 0.9% Sodium Chloride Injection, USP, 20 mL single-dose vial by Hospira, Inc. The label includes dosage information, usage as a sterile diluent, and storage instructions. The product is Rx only and features barcodes, lot numbers, and aseptic technique directions.*
FDA Label Image

Principal Display Panel (3 mL Cartridge Label)

Principal Display Panel (3 mL Cartridge Label)
Label for 0.9% Sodium Chloride Injection, USP, 50 mL single-dose vial by Hospira, Inc. The preservative-free saline solution is indicated for use as a sterile diluent. Label includes concentration, volume, product type, and distributor information with lot and expiration date placeholders.*
FDA Label Image

Principal Display Panel (3 mL Cartridge Container Label)

Principal Display Panel (3 mL Cartridge Container Label)
Label for 0.9% Sodium Chloride Injection, USP, 50 mL single-dose vial by Hospira, Inc. The label includes usage information as a sterile diluent, manufacturer details, and storage instructions. The product is marked Rx only.*
FDA Label Image

Sodiumchloride 08

Sodiumchloride 08
Label for Lifeshield 0.9% Sodium Chloride Injection, USP in a 10 mL single-dose vial. The preservative-free solution is a sterile diluent containing 9 mg sodium chloride per mL. Distributed by Hospira, Inc.*
FDA Label Image

Sodiumchloride 09

Sodiumchloride 09
Packaging label for Sodium Chloride 0.9% Injection, USP, 10 mL single-dose vial by Hospira, Inc. The label indicates the product is for use as a sterile diluent and is Rx only. It includes dosage information, storage instructions, and barcode details. The label also features the Lifeshield vial trademark and NDC 0409-4888-12.*
FDA Label Image

Sodiumchloride 10

Sodiumchloride 10
Label for Sodium Chloride 0.9% Injection, USP in a 2 mL single-dose carpule cartridge with luer lock, preservative-free. The label includes dosage markings up to 2 mL, designation as Rx only, barcodes, lot and expiration placeholders, and distributor Hospira, Inc., Lake Forest, IL.*
FDA Label Image

Sodiumchloride 11

Sodiumchloride 11
Label for 0.9% Sodium Chloride Injection, USP, 2 mL single-dose preservative-free cartridge units. Contains 50 Carpuject Sterile Cartridge Units with Luer Lock; needle not included. Distributed by Hospira, Inc. The label includes usage instructions, storage conditions, lot and expiration date placeholders, and barcode.*
FDA Label Image

Sodiumchloride 12

Sodiumchloride 12
Label for 3 mL single-dose Carpuject sterile cartridge unit of 0.9% Sodium Chloride Injection, USP. The label indicates it is preservative-free and includes a measurement scale in milliliters. It shows the product NDC 0409-1918-43, is marked Rx only, and displays lot and expiration date fields. The label is from Hospira, Inc., Lake Forest, IL.*
FDA Label Image

Sodiumchloride 13

Sodiumchloride 13
Label for Sodium Chloride 0.9% Injection, USP, 3 mL single-dose preservative-free sterile cartridge units packaged as 25 Carpuject units with Luer Lock. The label states it is for use with Carpuject holders, distributed by Hospira, Inc. It includes storage instructions, barcodes, and lot and expiration placeholders. Needle not included.*
FDA Label Image

Sodiumchloride 14

Sodiumchloride 14
Label for Sodium Chloride 0.9% Injection, USP, 5 mL single-dose sterile cartridge unit with Luer Lock, preservative-free. The label includes volume markings from 0.5 to 5 mL, the NDC 0409-1918-45, distributor Hospira, Inc., and placeholder text for lot number and expiration date.*
FDA Label Image

Sodiumchloride 15

Sodiumchloride 15
Label for 0.9% Sodium Chloride Injection, USP 5 mL single-dose sterile cartridge units. The preservative-free product is supplied as 25 Carpuject sterile cartridges with Luer Lock by Hospira, Inc. It includes storage instructions and usage warnings, with a barcode and lot/expiration placeholders visible.*

* 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.