Hs Logo (How Supplied Logo)
Sodium Chloride Injection, Solution
Product Images NDC 51662-1464
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 Sodium Chloride (NDC 51662-1464). 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.
Product Images & Figures Index
How Supplied (How Supplied)
A data table listing various units of sale and concentrations for sodium chloride injection solution. It includes different packaging types like single-dose cartridges and plastic fliptop vials, with volumes ranging from 2 mL to 50 mL, all at a 0.9% concentration.*
Logo (Logo)
Serialized Labeling (Serialized Labeling)
Partial view of a Sodium Chloride injection solution bottle label showing text indicating a 20 mL single-dose container. The label includes 0.9% Sodium Chloride Injection, USP and references use as a sterile diluent. There is a barcode with numeric codes and distributor information for HF Acquisition Co., LLC, Mukilteo, WA. The bottle has a gray aluminum seal with a yellow flip cap.*
Vial Label Opt 2 (Vial Label Opt 2)
Label of 0.9% Sodium Chloride Injection, USP, 20 mL single-dose vial. The preservative-free solution is indicated for sterile diluent use. The label shows active ingredient strength as 9 mg/mL sodium chloride and includes manufacturer Hospira, Inc. Distributed by Hospira in Lake Forest, Illinois. It also notes Rx only and includes NDC code 0409-4888-03.*
Viallabel Opt 1 (Vial Label Opt 1)
Label for 0.9% Sodium Chloride Injection, USP, 9 mg/mL solution in a 20 mL single-dose vial. The label states it is preservative-free and sterile, manufactured for Hospira, Inc., with the NDC 0409-4888-03. It includes a barcode area and mixing of black and green (PMS 583) text with instructions for use as a sterile diluent.*
Vial Label Opt 3 (Vial Label Opt 3)
Label for 0.9% Sodium Chloride Injection, USP, a sterile injectable solution. The label indicates a 20 mL single-dose vial, preservative-free, distributed by Hospira, Inc. It contains 9 mg/mL sodium chloride with possible pH adjustments. The label includes batch coding information fields for LOT and EXP.*
Vial Label Opt 4 (Vial Label Opt 4)
Label for 0.9% Sodium Chloride Injection, USP, 20 mL single-dose vial. The preservative-free solution contains 9 mg/mL sodium chloride and is indicated for use as a sterile diluent. Distributed by Hospira, Inc., Lake Forest, IL. Includes barcode and regulatory information.*
Vial Label Opt 5 (Vial Label Opt 5)
Label for 0.9% Sodium Chloride Injection, USP, 20 mL single-dose vial. It is preservative-free and sterile. The label includes the concentration of sodium chloride at 9 mg/mL and states it is for injection use. Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. The label features lot number and expiration date placeholders.*
* 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.
