Product Images 7.5% Sodium Bicarbonate

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Product Label Images

The following 7 images provide visual information about the product associated with 7.5% Sodium Bicarbonate NDC 51662-1463 by Hf Acquisition Co Llc, Dba Healthfirst, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

PRINCIPAL DISPLAY PANEL - 51662-1472-1 CARTON LABEL - 1472 CARTON LABEL

PRINCIPAL DISPLAY PANEL - 51662-1472-1 CARTON LABEL - 1472 CARTON LABEL

PRINCIPAL DISPLAY PANEL - 51662-1472-1 SERIALIZED CARTON LABELING - 1472 SERIALIZED CARTON LABELING

PRINCIPAL DISPLAY PANEL - 51662-1472-1 SERIALIZED CARTON LABELING - 1472 SERIALIZED CARTON LABELING

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.*

51662-1463-1 CARTON LABEL - CARTON LABELING

51662-1463-1 CARTON LABEL - CARTON LABELING

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.*

51662-1463-1 SERIALIZED CARTON LABELING - SERIALIZED CARTON

51662-1463-1 SERIALIZED CARTON LABELING - SERIALIZED CARTON

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.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.