Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED 0.9% Sodium Chloride Injection USP is supplied sterile and nonpyrogenic in glass ampoule container. NDC Size 0264-9375-88 10 mL Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. It is recommended that the product be stored at room temperature (25°C); however, brief exposure up to 40°C does not adversely affect the product. Revised: May 2018 Directions for Use of Ampoule To open ampoules, using gauze, place thumb and forefinger on color line, break at constriction. NOTE: Before use, perform the following checks: Inspect each container. Read the label. Ensure solution is the one ordered and is within the expiration date. Invert container and carefully inspect the solution in good light for cloudiness, haze, or particulate matter. Any container which is suspect should not be used. Use only if solution is clear and container and seals are intact.; PRINCIPAL DISPLAY PANEL NDC 0264-9375-88 0.9% Sodium Chloride Injection USP 10 mL Single-dose ampoule. Discard unused portion. Calc. Osmolarity: 0.308 mOsmol/mL For dilution of medication. For intravenous use. Use only if solution is clear. PRESERVATIVE-FREE Protect from freezing. Store at room temperature (25°C). Rx only Manufactured for: B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA Produced in Germany, API from Denmark. LD-521-A-4 LOT EXP 10 mL Ampoule Bottle label
- HOW SUPPLIED 0.9% Sodium Chloride Injection USP is supplied sterile and nonpyrogenic in glass ampoule container. NDC Size 0264-9375-88 10 mL Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. It is recommended that the product be stored at room temperature (25°C); however, brief exposure up to 40°C does not adversely affect the product. Revised: May 2018 Directions for Use of Ampoule To open ampoules, using gauze, place thumb and forefinger on color line, break at constriction. NOTE: Before use, perform the following checks: Inspect each container. Read the label. Ensure solution is the one ordered and is within the expiration date. Invert container and carefully inspect the solution in good light for cloudiness, haze, or particulate matter. Any container which is suspect should not be used. Use only if solution is clear and container and seals are intact.
- PRINCIPAL DISPLAY PANEL NDC 0264-9375-88 0.9% Sodium Chloride Injection USP 10 mL Single-dose ampoule. Discard unused portion. Calc. Osmolarity: 0.308 mOsmol/mL For dilution of medication. For intravenous use. Use only if solution is clear. PRESERVATIVE-FREE Protect from freezing. Store at room temperature (25°C). Rx only Manufactured for: B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA Produced in Germany, API from Denmark. LD-521-A-4 LOT EXP 10 mL Ampoule Bottle label
Overview
Each 1 mL of 0.9% Sodium Chloride Injection USP contains: Sodium Chloride USP 9 mg Water for Injection USP qs pH: 5.6 (4.5-7.0) Calculated Osmolarity: 0.308 mOsmol/mL pH adjusted with Hydrochloric Acid NF Concentration of Electrolytes (mEq/liter): Sodium 154 Chloride 154 0.9% Sodium Chloride Injection USP is sterile, nonpyrogenic, isotonic and contains no bacteriostatic or antimicrobial agents. The formula of the active ingredient is: Ingredient Molecular Formula Molecular Weight Sodium Chloride USP NaCI 58.44 Not made with natural rubber latex, PVC or DEHP.
Indications & Usage
0.9% Sodium Chloride Injection USP is indicated as pharmaceutic aid and diluent for the infusion of compatible drug additives. Refer to prescribing information accompanying additive drugs.
Dosage & Administration
This solution is for intravenous use only. Dosage is to be directed by a physician and is dependent upon age, weight, clinical condition of the patient and laboratory determinations. Frequent laboratory determinations and clinical evaluation are essential to monitor changes in blood glucose and electrolyte concentrations, and fluid and electrolyte balance during prolonged parenteral therapy. In the average adult, daily requirements of sodium and chloride are met by the infusion of one liter of 0.9% sodium chloride (154 mEq each of sodium and chloride). There is no specific pediatric dose. The dose is dependent on weight, clinical condition and laboratory results. Follow recommendations of appropriate pediatric reference text. (See PRECAUTIONS, Pediatric Use . ) Fluid administration should be based on calculated maintenance or replacement fluid requirements for each patient. 0.9% Sodium Chloride Injection USP may also be administered intravascularly as a priming fluid in hemodialysis procedures. When Sodium Chloride Injections USP are used as diluents for infusion of compatible drug additives, refer to dosage and administration information accompanying additive drugs. Some additives may be incompatible. Consult with pharmacist. When introducing additives, use aseptic techniques. Mix thoroughly. Do not store. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Warnings & Precautions
WARNINGS The administration of intravenous solutions can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentration. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentration. Solutions containing sodium ions should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there is sodium retention with edema. In patients with diminished renal function, administration of solutions containing sodium ions may result in sodium retention. Infusion of isotonic (0.9%) sodium chloride during or immediately after surgery may result in excessive sodium retention. Use the patient’s circulatory system status as a guide.
Contraindications
This solution is contraindicated where the administration of sodium or chloride could be clinically detrimental.
Adverse Reactions
Reactions which may occur because of the solution, added drugs or the technique of reconstitution or administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia. Carefully review the prescribing information for the diluted drug. The physician should also be alert to the possibility of adverse reactions to drug additives. Prescribing information for drug additives to be administered in this manner should be consulted. Symptoms may result from an excess or deficit of one or more of the ions present in the solution; therefore, frequent monitoring of electrolyte levels is essential. Hypernatremia may be associated with edema and exacerbation of congestive heart failure due to the retention of water, resulting in an expanded extracellular fluid volume. If infused in large amounts, chloride ions may cause a loss of bicarbonate ions, resulting in an acidifying effect. If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.
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