Bacteriostatic Sodium Chloride 0.9% Injection Multiple Dose Vials are used as a diluent for medications, providing a sterile solution for injection. They contain benzyl alcohol as a preservative to prevent bacterial growth, allowing multi-dose usage. This solution is employed for diluting or dissolving medications for intravenous, intramuscular, or subcutaneous administration. It helps maintain the isotonicity of drug solutions, ensuring safe medication delivery. Commonly used in clinical settings, it aids in administering consistent and effective treatment across various medical applications.
Details and Features:
Volume: 20 mL per vial
Packaging: 25 vials per pack
Concentration: 0.9% Sodium Chloride
Preservative: Contains benzyl alcohol (0.9%) as a bacteriostatic agent
Intended Use: Diluting or dissolving medications for injection
Multiple-dose vial: Allows multiple withdrawals for various dilutions or preparations
Mechanism of Action:
The primary role of Bacteriostatic Sodium Chloride 0.9% Injection is to act as a vehicle for the administration of medications. It provides a sterile solution in which drugs can be diluted without compromising their efficacy. The sodium chloride provides isotonicity, making it compatible with the body's extracellular fluids. The added benzyl alcohol prevents bacterial growth, thus permitting multiple uses from the same vial under appropriate conditions.
Warnings:
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Not For Direct Intravenous Use: This product must not be administered intravenously without proper dilution with other compatible medications, as it is intended solely as a diluent.
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Benzyl Alcohol Warning: The presence of benzyl alcohol can cause serious side effects in certain populations, such as neonates, and should be used cautiously in pregnant women or individuals with known allergies to benzyl alcohol.
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Consultation Required: Only use as directed by a healthcare provider and ensure compatibility with the medication to be diluted.
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Reuse Limitation: Intended for multiple use by a single individual, ensuring sterility is maintained during each access to the product. Always wipe the rubber stopper with an antiseptic before puncture.
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Storage: Maintain in a suitable environment, protecting it from light and freezing.
Side Effects:
- The solution itself is typically well-tolerated when used as directed for preparation, but side effects can arise from:
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Allergic Reactions: Potential hypersensitivity to ingredients, including benzyl alcohol.
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Local Reactions: Site irritation could occur if the product is improperly administered.
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Systemic Issues: If used in large quantities due to benzyl alcohol, it could cause metabolic complications in vulnerable groups, such as infants ("gasping syndrome").
Always ensure that the product is used in line with medical guidance and drilled protocol to prevent adverse effects connected to its administration.
- Medication reconstitution: Intended to dissolve lyophilised (freeze-dried) injectable medications before IM, IV (with dilution), or SC administration in clinic and hospital settings
- Aesthetic medicine: Used for botulinum toxin (e.g., Botox) reconstitution in medspa and cosmetic dermatology settings; the 0.9% benzyl alcohol content provides a mild local anaesthetic effect, which published literature associates with reduced injection discomfort versus preservative-free saline
- Hormone therapy and peptide preparation: Suitable as a diluent for peptide compounds and hormone therapy injectables, where an isotonic bacteriostatic vehicle is specified by the drug manufacturer
- High-volume clinical environments: The multiple-dose vial format supports sequential drug preparation across a session, reducing per-dose material cost in settings with frequent injection procedures
- EMS and emergency responder use: Applicable wherever field or facility-based medication dilution requires a preserved, isotonic diluent vehicle — confirm compatibility with specific drug protocols
- Dental and veterinary applications: May be used as a diluent in dental anaesthetic preparation or veterinary injectable compounding where bacteriostatic isotonic saline is indicated
This product is intended for use by qualified healthcare professionals or under the guidance of a licensed medical provider. It is not a substitute for professional medical advice, diagnosis, or treatment.
Rx-Only: This product is classified as a prescription-only (Rx) pharmaceutical and is intended exclusively for purchase and use by licensed healthcare professionals or under the supervision of a licensed medical provider. A valid professional licence is required to complete the purchase.
Not Medical Advice: The content on this page is provided for informational and procurement purposes only. It does not constitute medical advice, clinical guidance, diagnosis, or treatment recommendations. Healthcare professionals should consult current prescribing information, institutional protocols, and applicable clinical guidelines before use.
YMYL Notice: Information on this page pertains to a prescription injectable pharmaceutical product. All clinical claims on this page are supported by FDA prescribing information, USP monograph standards, and peer-reviewed literature. This content has been prepared with reference to authoritative sources; however, it should not replace direct consultation of the current FDA-approved prescribing information supplied with the product.
Manufacturer Information: Product manufactured by Hospira, Inc., a Pfizer company. Regulatory standing, NDC classification, and prescribing information are the responsibility of the manufacturer. Mountainside Medical makes no independent representations regarding manufacturer certifications beyond what is stated in the manufacturer's official product documentation.
Regulatory: This product is subject to applicable federal and state regulations governing the purchase, handling, storage, and administration of prescription pharmaceutical products in the United States.