51662 1256 1 Serialized Labeling
8.4% Sodium Bicarbonate Injection, Solution
Product Images NDC 51662-1256
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Product Visual Gallery
This gallery contains 11 technical images submitted to the FDA as part of the official labeling for 8.4% Sodium Bicarbonate (NDC 51662-1256). 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
Serialized Label (51662 1256 1 Sodium Bicarbonate 50 Serialized Label)
Not available. The given text seems to be a combination of a barcode and a product code, with some additional information about the manufacturer and distributor.*
51662 1256 2 Pouch Label Update April 2021
Sodium Bicarbonate Injection is a sterile solution used for intravenous administration. Each 50mL vial contains 50 milliequivalents of Sodium Bicarbonate USP at a concentration of 8.4%. It is important to discard any unused portion and not to resterilize. The injection should be clear and the seal should be intact and undamaged. If there is any precipitate, it should not be used. The stopper should be cleansed with antiseptic before use. The solution should be stored at room temperature and protected from freezing. This product is distributed by HF Acquisition Co., LLC and should only be used under prescription. Detailed information can be found in the manufacturer's package insert.*
51662 1256 3 Case Label Update April 2021
Sodium Bicarbonate Injection USP is a sterile solution containing 8.4% of sodium bicarbonate. It is available in a 50mL vial and is supplied in boxes of 25. The National Drug Code (NDC) for the product is 51662-1256-3 and the lot number is 12345, with an expiration date of January 1, 2030. The product should only be used if the solution is clear and the seal is intact and undamaged. Users should discard any unused portion and not attempt to resterilize the injection. The injection should not be used if it contains any precipitate. The stopper should be cleansed with antiseptic prior to use. The product should be stored between 20-25°C (68-77°F), and should not be frozen. The manufacturer's package insert should be consulted for additional information. The original manufacturer's NDC is 0409-6625-14. The product is available for prescription use only and is distributed by HF Acquisition Co., LLC, located in Mukilteo, Washington.*
5166212562 Label Sodium Bicarb
This is a description of a medication with the NDC code 51662-1256-2. The medication is contained in a 50mL vial and has an expiration date of June 1st, 2027. The packaging should not be opened if it appears damaged, and the injection should not be used if it contains precipitate. The medication should be stored at a temperature between 20 to 25C (68 to 77F). The manufacturer's package insert should be consulted. The medication was originally manufactured with the NDC code 0409-6625-02 and is distributed by HF Acquisition Co., LLC.*
5166212563 Rfid Label Sodium Bicarb
The provided text seems to be a product identifier, a reference to a package insert, and the name and location of the distributor. Without further information about the product, its purpose or its manufacturer, it is not possible to provide a more accurate description.*
5166212563 Label Sodium Bicarb
This is a description of a medication called 8.4% Sodium Bicarbonate that comes in a 50mL vial with a strength of 50mEq per milliliter. The box contains 25 vials, and the lot number is ABCDEFGHIJKLMNOPQRST with an expiration date of June 1, 2021. The medication is for intravenous use only and should only be used if the seal is intact and the solution is clear. There should be no precipitate in the injection. It should be stored at 20 to 25°C. The package insert should be consulted for further information. The medication is distributed by HF Acquisition Co, LLC in Mukilteo, WA 98275.*
How Supplied (How Supplied)
This is a table representing various dosages and concentrations of medication in different forms of containers including syringes, vials and LVP glass. The columns indicate the amount of medication in mg/mL, mEq/mL, mEq/container, pH level, form, (NaHCO3), (Na+), (HCO3), size in mL, List No., concentration, % i, and mOsmol. There are also different types of medications listed for different ages and conditions.*
Vial (Sodium Bicarb Vial Label)
This is a description of a 50mL single-dose container of sodium bicarbonate solution manufactured by Hospira, Inc. The solution contains 50mEq of sodium bicarbonate with a concentration of 1 mEq/mL and has a total of 4.2g of sodium bicarbonate with 84mg/mL. It is for intravenous use only and is sterile and nonpyrogenic. The usual dose is not specified, but instructions are provided to not use the solution if the seal is damaged or if the solution contains any precipitate. The solution has a pH range of 7.0 to 8.5 and each mL contains 84mg of sodium bicarbonate. The container does not contain any bacteriostat and must be discarded if unused. The NDC number is 0409-6625-02.*
Vial Label Update April 2021
NDC 0409-6625-22 is a sterile and nonpyrgenic injection containing Sodium Bicarbonate. It comes in a single-dose vial of 50 mL with a concentration of 8.4% (50 mEq/50 mL or 1 mEg/mL) for intravenous use only. Each mL contains 84 mg of sodium bicarbonate in water for injection. The pH of the solution ranges from 1.0 to 8.5 and may be adjusted using carbon dioxide or nitrogen. It has no bacteriostat and should be discarded after single-use. The recommended dosage is mentioned in the insert. Provided it is clear and intact, the injection should be used if the seal is unbroken. It should be stored at a temperature between 20°C to 25°C (66°F to 77°F) and protected from freezing. The product is distributed by Hospira, Inc. in the USA. RL-7728.*
Vial Label
NDC 0409-6625-22 is a sodium bicarbonate injection used for Intravenous use. It is a single-dose vial, sterile and non-pyrogenic. The dosage depends on the insert. It is only recommended to use if seal is intact and undamaged or else contain precipitate. It must be stored at controlled room temperature and protected from freezing. This product is distributed by Hospira Inc, Lake Forest, USA.*
* 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.
