FDA
Sodium Chloride 0.9% in Plastic Container
The FDA lists this product in 46 strengths and forms.
Indications
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.
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.
Composition
- Active ingredients
- SODIUM CHLORIDE 27MG/3ML (9MG/ML)
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- SODIUM CHLORIDE 900MG/100ML · SolutionNDA017427-001 · Prescription
- SODIUM CHLORIDE 180MG/20ML (9MG/ML) · SolutionANDA088912-002 · Prescription
- SODIUM CHLORIDE 270MG/30ML (9MG/ML) · SolutionANDA088912-003 · Prescription
- SODIUM CHLORIDE 90MG/10ML (9MG/ML) · SolutionANDA088912-001 · Prescription
- SODIUM CHLORIDE 18MG/2ML (9MG/ML) · Solution



