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EXPIRATION DATE: 31 AUG 2027
Hospira Bacteriostatic Sodium Chloride for injection USP is a sterile, multiple-dose vial from which repeated withdrawals may be made to dilute or dissolve drugs and medication.
Each milliliter (ml) contains sodium chloride 9 mg and 0.9% (9mg/ml) benzyl alcohol added as a bacteriostatic preservative.
May contain hydrochloric acid for pH adjustment. The pH is 5.3 (4.5 to 7.0).
Bacteriostatic Sodium Chloride differs from bacteriostatic water in that it contains added NaCl.
**Bacteriostatic Water has no added sodium chloride.
The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.
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Please note that this product ships WITHOUT temperature control packaging.
This item is to be stored at room temperature per manufacturer’s instruction.
To limit exposure to extreme temperatures that may affect this product while in transit we recommend choosing Next Day Air delivery when selecting your shipping method.
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Please review our shipping notices and product-use acknowledgement before continuing.
Orders will be shipped out Monday–Friday until 2:00 PM CST.
We currently ship within the United States only.
Note: USPS Ground Advantage can take 7–9 business days to some ZIP codes. Choose expedited shipping if you are on a deadline.
Syringe Needle Depot cannot determine the cause of cloudiness, clumping, precipitation, discoloration, or failed reconstitution after a diluent has been mixed with any third-party peptide, compound, powder, vial, or other material.
These outcomes may result from variables outside our control, including peptide quality, handling, contamination, storage, reconstitution technique, pH, or formulation incompatibility.
Syringe Needle Depot does not manufacture, test, authenticate, or guarantee the quality or compatibility of any third-party peptide or compound used with our products.
A cloudy, clumped, precipitated, or otherwise unsuccessful mixture does not, by itself, establish that the diluent was defective, contaminated, improperly formulated, or unsuitable.