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Dragon Pharma Bacteriostatic Water for Injection, Sterile Vial
Dragon Pharma

Dragon Pharma Bacteriostatic Water for Injection, Sterile Vial

Injection · 0.9% · vial

In stock · ships within 24h Out of stock
$20.00

Bacteriostatic Water is sterile water for injection with 0.9% benzyl alcohol added as a bacteriostatic preservative, supplied in a multiple-dose vial. It is used to dilute or dissolve drugs and powders that must be reconstituted before injection.

GMP-manufactured, each batch HPLC-verified with a Certificate of Analysis on file. Bacteriostatic Water for sale with U.S. domestic and international shipping.

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Product overview

Bacteriostatic Water for Injection and Reconstitution

Bacteriostatic Water is sterile, nonpyrogenic water for injection containing 0.9% (9 mg/mL) of benzyl alcohol added as a bacteriostatic preservative. It comes in a multiple-dose vial from which repeated withdrawals can be made, and that preservative is what separates it from plain sterile water: the contents stay protected across several preparations. In this catalog it is the diluent used to reconstitute powders such as somatropin, Cagrilintide and Survodutide vials, and the oral products on the Cialis page need no diluent at all.

  • 0.9% (9 mg/mL) benzyl alcohol as the bacteriostatic preservative
  • Multiple-dose vial - repeated withdrawals
  • Sterile and nonpyrogenic water for injection
  • HPLC-verified - batch-tested, COA on file

How It Is Used

The label states the preparation is designed solely for parenteral use after the addition of a drug that requires dilution or must be dissolved in an aqueous vehicle before injection. Each preparation follows the manufacturer's instructions for the drug being reconstituted, including the route and the volume. It is not a fluid replacement and must be made approximately isotonic before use, because intravenous administration without a solute may cause hemolysis.

Dosage & Administration

There is no fixed dose: the volume is set by the product being reconstituted and by its own instructions. The label warns that solutions containing benzyl alcohol must not be used in neonates, that they should not be used for fluid replacement, and that they must not be used in epidural or spinal procedures. Store the vial at room temperature, and inspect any reconstituted solution for clarity and freedom from particles before use.

Quality & Authenticity

Every batch is produced under GMP conditions and checked by third-party HPLC, with a Certificate of Analysis held for the batch. The vial arrives sealed with a batch code to check before use.

Prescription medicine: consult a healthcare professional before use.

Specifications

Trade NameBacteriostatic Water
Generic NameWater for injection with 0.9% benzyl alcohol
ManufacturerDragon Pharma
Dosage0.9% (9 mg/mL) benzyl alcohol
PackageMultiple-dose vial
Drug ClassSterile diluent and reconstitution vehicle
AdministrationFor diluting or dissolving drugs for injection
StorageRoom temperature, away from moisture and direct light
Prescription StatusPrescription medicine
VerificationThird-party HPLC per batch, COA on file
ShippingU.S. domestic and international shipping

Stacks

With Lyophilised Powders

Used to reconstitute powders that arrive dry, such as somatropin and research peptides, following the volume stated for each product.

The preservative allows more than one withdrawal from the same vial, so a multi-dose preparation keeps working between sessions.

Where It Must Not Be Used

Not for neonates: benzyl alcohol is toxic in that group, and preservative-free sterile water is used instead. Not for fluid replacement, and not for epidural or spinal procedures.

Never given on its own, and never intravenously without a solute that makes the mixture approximately isotonic.

Prescription medicine. Compatibility notes above follow the FDA labeling for Bacteriostatic Water for Injection and are not medical advice; consult a healthcare professional.

FAQ

Before you ask

Questions, answered

Bacteriostatic Water for Injection, USP is used to dilute or dissolve drugs that need an aqueous vehicle before injection. In practice it reconstitutes lyophilised powders such as somatropin and research peptides, where a measured volume is added to the dry vial. The benzyl alcohol preservative allows repeated withdrawals from the same multiple-dose vial, which is the difference from plain sterile water.
The label describes it as a sterile, nonpyrogenic preparation of water for injection containing 0.9% (9 mg/mL) of benzyl alcohol added as a bacteriostatic preservative, with a pH of 5.7 in a range of 4.5 to 7.0. Water for injection is chemically H2O. The 0.9% figure is the concentration of the preservative, not of salt, and the catalog page lists the concentration as 0.9% for this vial.
There is no fixed dose. The volume is set by the product being reconstituted and by the manufacturer's instructions for that product, which state the amount of diluent and the intended route. That is why the label tells the user to consult the manufacturer's instructions for the choice of vehicle and the appropriate dilution before preparing anything.
No. The label states that solutions containing benzyl alcohol must not be used in neonates because of benzyl alcohol toxicity, and that preservative-free sterile water is used instead in that group. It must not be used for fluid replacement, and it must not be used in epidural or spinal anaesthesia procedures. Intravenous administration without a solute may cause hemolysis, so it must be made approximately isotonic first.
No. It is a diluent, not a treatment. The label says the preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to the instructions of the manufacturer of the drug being administered. It is added to the product being prepared, and the resulting solution is what gets used.
Yes. Bacteriostatic Water is stocked here in sealed vials with U.S. domestic and international delivery, and the page above shows current availability and price for both destinations. Every batch is produced under GMP conditions and checked by third-party HPLC with the Certificate of Analysis on file, so the vial can be checked against its batch documentation when it arrives.
On its own it is a diluent, not an active drug, so any effect comes from the substance it dissolves. The benzyl alcohol preservative can irritate tissue at the site of injection, and the solution is not suitable for anyone allergic to benzyl alcohol or for newborns. Discard the vial if the liquid turns cloudy or shows particles, and follow the storage note printed on the label.
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