Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED Sodium Chloride Injection USP, 0.9% is supplied in the following: 2 mL vials packaged in carton of 25 vials (NDC 0641-0497-25) 10 mL vials packaged in carton of 25 vials (NDC 0641-6144-25) Storage Store at 20° - 25°C (68°-77°F), excursions permitted to 15° - 30°C (59° - 86°F) [See USP Controlled Room Temperature]. Avoid freezing.; PRINCIPAL DISPLAY PANEL NDC 0641- 0497 -17 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL Preservative Free For use as a sterile diluent 2 mL Single Dose Vial NDC 0641- 0497 -25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL Preservative Free For use as a sterile diluent 25 x 2 mL Single Dose Vials vial shelfpack; PRINCIPAL DISPLAY PANEL NDC 0641-6144-01 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 10 mL Single Dose Vial Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 25 x 10 mL Single Dose Vials Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-01 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 10 mL Single Dose Vial Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 25 x 10 mL Single Dose Vials Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature].
- HOW SUPPLIED Sodium Chloride Injection USP, 0.9% is supplied in the following: 2 mL vials packaged in carton of 25 vials (NDC 0641-0497-25) 10 mL vials packaged in carton of 25 vials (NDC 0641-6144-25) Storage Store at 20° - 25°C (68°-77°F), excursions permitted to 15° - 30°C (59° - 86°F) [See USP Controlled Room Temperature]. Avoid freezing.
- PRINCIPAL DISPLAY PANEL NDC 0641- 0497 -17 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL Preservative Free For use as a sterile diluent 2 mL Single Dose Vial NDC 0641- 0497 -25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL Preservative Free For use as a sterile diluent 25 x 2 mL Single Dose Vials vial shelfpack
- PRINCIPAL DISPLAY PANEL NDC 0641-6144-01 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 10 mL Single Dose Vial Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 25 x 10 mL Single Dose Vials Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-01 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 10 mL Single Dose Vial Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature]. NDC 0641-6144-25 Rx only Sodium Chloride Injection USP, 0.9% 0.308 mOsmol/mL PRESERVATIVE-FREE For use as a sterile diluent 25 x 10 mL Single Dose Vials Each mL contains sodium chloride 9 mg in Water for Injection; pH 4.5-7.0, may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. Sterile, nonpyrogenic. Contains no preservative. Discard unused portion. For additional information, see package insert. Store at 20º-25ºC (68º-77ºF) [See USP Controlled Room Temperature].
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, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. Its chloride and sodium ion concentrations are approximately 0.154 mEq of each per milliliter and its calculated osmolality is 0.308 milliosmols per mL. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment, pH 5.3 (4.5 to 7.0). Sodium chloride, USP occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. The empirical formula for sodium chloride is NaCl, and the molecular weight is 58.44.
Indications & Usage
This parenteral preparation 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.
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 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.
Similar Drugs
Related medications based on brand, generic name, substance, active ingredients.