Infant 4.2% Sodium Bicarbonate Injection, Solution
Product Images NDC 51662-1310

3 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Infant 4.2% Sodium Bicarbonate (NDC 51662-1310). 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

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing various dosage forms, concentrations, and content details for sodium bicarbonate products. It includes descriptions like Abbocject Syringe, Fliptop Vial, and LVP Glass Container, with corresponding concentration percentages, pH ranges, and container sizes. The table specifically highlights the Infant Abbocject Syringe with 4.2% concentration and 42 mg/mL.*
FDA Label Image

Serialized Label (Serialized 51662 1310 1 Sodium Bicarb 4.2)

Serialized Label (Serialized 51662 1310 1 Sodium Bicarb 4.2)
Box packaging of INFANT 4.2% Sodium Bicarbonate injection, USP in a 10 mL glass vial. The label shows the strength as 4.2%, equivalent to 5 mEq/10 mL or 0.5 mEq/mL, for intravenous use. The product contains an Abbocject unit of use syringe with a male luer lock adapter and 20-gauge protected needle. Distributed by HF Acquisition Co. LLC, Mukilteo, WA.*
FDA Label Image

Syringe Label (Syrnge Label)

Syringe Label (Syrnge Label)
Label for INFANT 4.2% SODIUM BICARBONATE Injection, USP, a 10 mL single-dose intravenous solution with 42 mg/mL strength. The label shows dosing information, barcode, NDC 0409-5534-34, and manufacturer Hospira, Inc.*

* 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.