Pediatric 8.4% Sodium Bicarbonate Injection, Solution
Product Images NDC 51662-1472

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Pediatric 8.4% Sodium Bicarbonate (NDC 51662-1472). 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

Principal Display Panel (51662-1472-1 CARTON LABEL)

FDA Label Image

Principal Display Panel (51662-1472-1 SERIALIZED CARTON LABELING)

FDA Label Image

51662-1472-1 Syringe Label (1472 Syringe Label)

51662-1472-1 Syringe Label (1472 Syringe Label)
This is a medical product for pediatric use that contains 8.4% Sodium Bicarbonate. It comes in a 10 mL single-dose form and has a usual dosage specified in the insert. The product is sterile, nonpyrogenic and is meant for intravenous use. The product has packaging graphics, and a label control approval. The manufacturing location of the product is Hospis, Lake Forest in the United States.*
FDA Label Image

51662-1463-1 Carton Label (Carton Labeling)

FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
This is a list of product numbers, dosage forms, concentration percentages, milligrams (mg), milliequivalents (mEq) per milliliter (mL) and/or per container. It also includes mOsmol and pH values for different types of syringes and vials.*
FDA Label Image

51662-1463-1 Serialized Carton Labeling (Serialized Carton)

FDA Label Image

51662-1463-1 Syringe Label (Syringe Label)

51662-1463-1 Syringe Label (Syringe Label)
This is a description of a medication product containing 7.5% Sodium Bicarbonate. It is available in a single-dose 50 mL injection, and the usual dosage can be found in the insert. It is a sterile and nonpyrogenic solution, and any unused portion should be discarded. The product is manufactured by Hospira, Inc., located in Lake Forest, IL, USA. The packaging includes graphics art and a label with control number D-395.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.