Logo (How Supplied Logo)
Sodium Chloride Injection, Solution
Product Images NDC 51662-1342
6 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 51662-1342). 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.
How Supplied (How Supplied)
A data table listing various units of sale for 0.9% sodium chloride injection solutions, including single-dose cartridges with Luer Lock and single-dose plastic Fliptop vials. The table includes multiple package sizes ranging from 2 mL to 50 mL volume per unit.*
Labeled Vial (Labeled Vial)
SODIUM CHLORIDE 9 mg/mL injection solution in a 10 mL single-dose vial. The vial has a clear body with a light green flip-off cap and features printed text stating '0.9% Sodium Chloride Injection, USP'. The labeler is HF Acquisition Co LLC, DBA HealthFirst. This product is intended for intramuscular, intravenous, and subcutaneous use.*
Logo (Logo)
Serialized Labeling (Serialized Labeling On Vial)
Sodium Chloride 0.9% Injection, USP solution in a 10 mL single-dose glass vial with a green flip-off cap. The label displays the proprietary name, strength, dosage form, and indicates it is for use as a sterile diluent. Includes a barcode label with manufacturing and distribution information from HF Acquisition Co., LLC.*
Vial Label (Vial Label)
Label for 0.9% Sodium Chloride Injection, USP, a sterile diluent injection solution in a 10 mL single-dose vial. The label indicates the product is preservative-free and contains 9 mg of sodium chloride per mL. Manufactured by Hospira, Inc., Lake Forest, IL, USA, with NDC 0409-4888-02.*
* 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.
