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

7 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · 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)

Principal Display Panel (51662-1472-1 CARTON LABEL)
Packaging label for PEDIATRIC 8.4% SODIUM BICARBONATE injection, USP, 10 mEq (1 mEq/mL) in a 10 mL glass unit dose syringe. The label includes handling and aseptic technique instructions, a barcode, the Lifeshield brand, and is labeled for Rx use only. The product is from HF Acquisition Co LLC, DBA HealthFirst.*
FDA Label Image

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

Principal Display Panel (51662-1472-1 SERIALIZED CARTON LABELING)
Packaging label for PEDIATRIC 8.4% SODIUM BICARBONATE injection, USP, 10 mL unit of use syringe. The syringe is glass ABBOJECT with LifeShield technology, including a male luer lock adapter and 20-gauge protected needle. The label shows a concentration of 8.4% and is marked Rx only. The labeler is Hospira, distributed by HF Acquisition Co LLC.*
FDA Label Image

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

51662-1472-1 Syringe Label (1472 Syringe Label)
Label for PEDIATRIC 8.4% SODIUM BICARBONATE Injection, USP 10 mEq (1 mEq/mL) 10 mL single-dose vial. The sterile, nonpyrogenic solution is for intravenous use with a pH range of 7.0 to 8.5. Label includes bar code, manufacturer Hospira, Inc., Lake Forest, IL, and printing details with PMS color specifications.*
FDA Label Image

51662-1463-1 Carton Label (Carton Labeling)

51662-1463-1 Carton Label (Carton Labeling)
Packaging label for PEDIATRIC 8.4% SODIUM BICARBONATE Injection, USP, 7.5% strength with 44.6 mEq (0.9 mEq/mL) in a 50 mL glass unit of use syringe. The label indicates the product includes an Abbocject male luer lock adapter with 18-gauge protected needle, is for intramuscular use, and distributed by HF Acquisition Co LLC, DBA HealthFirst. Instructions for use and aseptic technique are also featured on the label.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table presenting various dosage forms and concentrations of sodium bicarbonate injections, including pediatric and infant-specific forms. Columns list dosage form, concentration percentage, strength in mg/mL and mEq/mL for sodium bicarbonate and ions, container size, osmolarity, and pH range for each listed product variant.*
FDA Label Image

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

51662-1463-1 Serialized Carton Labeling (Serialized Carton)
Packaging label for 7.5% Sodium Bicarbonate Injection, USP in a 50 mL unit of use syringe. The label highlights 44.6 mEq (0.9 mEq/mL) strength, with LifeShield glass and the ABBOJECT unit of use syringe featuring a male luer lock adapter and 18-gauge protected needle. It is marked Rx only and distributed by HF Acquisition Co LLC, DBA HealthFirst. The brand Hospira is also visible on the packaging.*
FDA Label Image

51662-1463-1 Syringe Label (Syringe Label)

51662-1463-1 Syringe Label (Syringe Label)
This packaging label displays a 50 mL single-dose vial of 7.5% Sodium Bicarbonate Injection, USP, with a concentration of 44.6 mEq (0.9 mEq/mL). The label includes dosing and sterility information, pH range of 8.0 (7.0 to 8.5), and manufacturer Hospira, Inc., Lake Forest, IL. The NDC number and barcode are also 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.