Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED: Sodium Chloride Injection, USP, 0.9%, preservative free, is available as follows: Product Code Unit of Sale Each 918602 63323-186-02 Unit of 25 NDC 63323-186-04 2 mL fill, in a 3 mL Single Dose vial 918610 63323-186-10 Unit of 25 NDC 63323-186-01 10 mL Single Dose vial 918620 63323-186-20 Unit of 25 NDC 63323-186-03 20 mL Single Dose vial Preservative Free. Discard unused portion. Use only if solution is clear and seal intact. Store at 20º to 25ºC (68º to 77ºF) [see USP Controlled Room Temperature] www.fresenius-kabi.com/us 45764F Revised: November 2020 Fresenius Kabi Logo; PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Label NDC 63323-186-04 918602 Sodium Chloride Injection, USP 0.9% 2 mL Single Dose Vial FOR DRUG DILUENT USE Preservative Free Rx only Discard unused portion. PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Label; PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Tray Label NDC 63323-186-02 918602 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 2 mL Single Dose Vials PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Tray Label; PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Label NDC 63323-186-01 918610 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 10 mL Single Dose Vial PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Label; PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Tray Label NDC 63323-186-10 918610 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 10 mL Single Dose Vials PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Tray Label; PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Label NDC 63323-186-03 918620 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 20 mL Single Dose Vial PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Label; PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Tray Label NDC 63323-186-20 918620 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 20 mL Single Dose Vials PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Tray Label
- HOW SUPPLIED: Sodium Chloride Injection, USP, 0.9%, preservative free, is available as follows: Product Code Unit of Sale Each 918602 63323-186-02 Unit of 25 NDC 63323-186-04 2 mL fill, in a 3 mL Single Dose vial 918610 63323-186-10 Unit of 25 NDC 63323-186-01 10 mL Single Dose vial 918620 63323-186-20 Unit of 25 NDC 63323-186-03 20 mL Single Dose vial Preservative Free. Discard unused portion. Use only if solution is clear and seal intact. Store at 20º to 25ºC (68º to 77ºF) [see USP Controlled Room Temperature] www.fresenius-kabi.com/us 45764F Revised: November 2020 Fresenius Kabi Logo
- PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Label NDC 63323-186-04 918602 Sodium Chloride Injection, USP 0.9% 2 mL Single Dose Vial FOR DRUG DILUENT USE Preservative Free Rx only Discard unused portion. PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Label
- PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Tray Label NDC 63323-186-02 918602 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 2 mL Single Dose Vials PACKAGE LABEL - PRINCIPAL DISPLAY - Sodium Chloride 2 mL Single Dose Vial Tray Label
- PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Label NDC 63323-186-01 918610 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 10 mL Single Dose Vial PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Label
- PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Tray Label NDC 63323-186-10 918610 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 10 mL Single Dose Vials PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 10 mL Single Dose Vial Tray Label
- PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Label NDC 63323-186-03 918620 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 20 mL Single Dose Vial PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Label
- PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Tray Label NDC 63323-186-20 918620 Sodium Chloride Injection, USP 0.9% FOR DRUG DILUENT USE Rx only 25 x 20 mL Single Dose Vials PACKAGE LABEL – PRINCIPAL DISPLAY – Sodium Chloride 20 mL Single Dose Vial Tray Label
Overview
This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Sodium Chloride Injection, USP, 0.9% is a sterile, nonpyrogenic solution. The osmolarity is 0.300 mOsmol/mL (calculated). Each mL contains: Sodium chloride 9 mg; Water for Injection q.s. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single dose containers. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment (pH 4.5-7.0). Sodium chloride occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. It is soluble in glycerin and slightly soluble in alcohol. The empirical formula for sodium chloride is NaCl and the molecular weight is 58.44.
Indications & Usage
: This parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular, or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.
Dosage & Administration
: The volume of the preparation to be used for diluting or dissolving any drug for injection, is dependent on the vehicle concentration, dose and route of administration as recommended by the manufacturer. This parenteral should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. See PRECAUTIONS .
Warnings & Precautions
No warnings available yet.
Adverse Reactions
Reactions which may occur because of this solution, added drugs or the technique of reconstitution or administration include febrile response, local tenderness, abscess, tissue necrosis or infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection and extravasation. If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate countermeasures and, if possible, retrieve and save the remainder of the unused vehicle for examination.
Drug Interactions
Some drugs for injection may be incompatible in a given vehicle, or when combined in the same vehicle or in a vehicle containing benzyl alcohol. Consult with pharmacist, if available. Use aseptic technique for single or multiple entry and withdrawal from all containers. When diluting or dissolving drugs, mix thoroughly and use promptly. Do not store reconstituted solutions of drugs for injection unless otherwise directed by the manufacturer of the solute. Do not use unless the solution is clear and seal intact. Do not reuse single dose containers, discard unused portion.
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