Reviews Sodium Chloride Injection


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Normal Saline Drug Description
SODIUM CHLORIDE
(sodium chloride) Injection
DRUG DESCRIPTION
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid
and electrolyte replenishment in single dose containers for intravenous administration.
It contains no antimicrobial agents. The nominal pH is 5.5 (4.5 to 7.0). Composition,
osmolarity, and ionic concentration are shown below:
0.45% Sodium Chloride Injection, USP contains 4.5 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 154 mOsmol/L (calc). It contains 77 mEq/L sodium
and 77 mEq/L chloride.
0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L
sodium and 154 mEq/L chloride.
The flexible container is made with non-latex plastic materials specially designed
for a wide range of parenteral drugs including those requiring delivery in containers
made of polyolefins or polypropylene. For example, the AVIVA container system
is compatible with and appropriate for use in the admixture and administration
of paclitaxel. In addition, the AVIVA container system is compatible with and
appropriate for use in the admixture and administration of all drugs deemed
compatible with existing polyvinyl chloride container systems. The solution
contact materials do not contain PVC, DEHP, or other plasticizers.
The suitability of the container materials has been established through biological
evaluations, which have shown the container passes Class VI U.S. Pharmacopeia
(USP) testing for plastic containers. These tests confirm the biological safety
of the container system. The flexible container is a closed system, and air
is prefilled in the container to facilitate drainage. The container does not
require entry of external air during administration.
The container has two ports: one is the administration outlet port for attachment
of an intravenous administration set and the other port has a medication site
for addition of supplemental medication (See Directions
for Use). The primary function of the overwrap is to protect the container
from the physical environment.Last reviewed on RxList: 4/20/2009




Normal Saline Drug Description
SODIUM CHLORIDE
(sodium chloride) Injection
DRUG DESCRIPTION
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid
and electrolyte replenishment in single dose containers for intravenous administration.
It contains no antimicrobial agents. The nominal pH is 5.5 (4.5 to 7.0). Composition,
osmolarity, and ionic concentration are shown below:
0.45% Sodium Chloride Injection, USP contains 4.5 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 154 mOsmol/L (calc). It contains 77 mEq/L sodium
and 77 mEq/L chloride.
0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L
sodium and 154 mEq/L chloride.
The flexible container is made with non-latex plastic materials specially designed
for a wide range of parenteral drugs including those requiring delivery in containers
made of polyolefins or polypropylene. For example, the AVIVA container system
is compatible with and appropriate for use in the admixture and administration
of paclitaxel. In addition, the AVIVA container system is compatible with and
appropriate for use in the admixture and administration of all drugs deemed
compatible with existing polyvinyl chloride container systems. The solution
contact materials do not contain PVC, DEHP, or other plasticizers.
The suitability of the container materials has been established through biological
evaluations, which have shown the container passes Class VI U.S. Pharmacopeia
(USP) testing for plastic containers. These tests confirm the biological safety
of the container system. The flexible container is a closed system, and air
is prefilled in the container to facilitate drainage. The container does not
require entry of external air during administration.
The container has two ports: one is the administration outlet port for attachment
of an intravenous administration set and the other port has a medication site
for addition of supplemental medication (See Directions
for Use). The primary function of the overwrap is to protect the container
from the physical environment.Last reviewed on RxList: 4/20/2009




Normal Saline Drug Description
SODIUM CHLORIDE
(sodium chloride) Injection
DRUG DESCRIPTION
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid
and electrolyte replenishment in single dose containers for intravenous administration.
It contains no antimicrobial agents. The nominal pH is 5.5 (4.5 to 7.0). Composition,
osmolarity, and ionic concentration are shown below:
0.45% Sodium Chloride Injection, USP contains 4.5 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 154 mOsmol/L (calc). It contains 77 mEq/L sodium
and 77 mEq/L chloride.
0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L
sodium and 154 mEq/L chloride.
The flexible container is made with non-latex plastic materials specially designed
for a wide range of parenteral drugs including those requiring delivery in containers
made of polyolefins or polypropylene. For example, the AVIVA container system
is compatible with and appropriate for use in the admixture and administration
of paclitaxel. In addition, the AVIVA container system is compatible with and
appropriate for use in the admixture and administration of all drugs deemed
compatible with existing polyvinyl chloride container systems. The solution
contact materials do not contain PVC, DEHP, or other plasticizers.
The suitability of the container materials has been established through biological
evaluations, which have shown the container passes Class VI U.S. Pharmacopeia
(USP) testing for plastic containers. These tests confirm the biological safety
of the container system. The flexible container is a closed system, and air
is prefilled in the container to facilitate drainage. The container does not
require entry of external air during administration.
The container has two ports: one is the administration outlet port for attachment
of an intravenous administration set and the other port has a medication site
for addition of supplemental medication (See Directions
for Use). The primary function of the overwrap is to protect the container
from the physical environment.Last reviewed on RxList: 4/20/2009




Normal Saline Drug Description
SODIUM CHLORIDE
(sodium chloride) Injection
DRUG DESCRIPTION
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid
and electrolyte replenishment in single dose containers for intravenous administration.
It contains no antimicrobial agents. The nominal pH is 5.5 (4.5 to 7.0). Composition,
osmolarity, and ionic concentration are shown below:
0.45% Sodium Chloride Injection, USP contains 4.5 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 154 mOsmol/L (calc). It contains 77 mEq/L sodium
and 77 mEq/L chloride.
0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L
sodium and 154 mEq/L chloride.
The flexible container is made with non-latex plastic materials specially designed
for a wide range of parenteral drugs including those requiring delivery in containers
made of polyolefins or polypropylene. For example, the AVIVA container system
is compatible with and appropriate for use in the admixture and administration
of paclitaxel. In addition, the AVIVA container system is compatible with and
appropriate for use in the admixture and administration of all drugs deemed
compatible with existing polyvinyl chloride container systems. The solution
contact materials do not contain PVC, DEHP, or other plasticizers.
The suitability of the container materials has been established through biological
evaluations, which have shown the container passes Class VI U.S. Pharmacopeia
(USP) testing for plastic containers. These tests confirm the biological safety
of the container system. The flexible container is a closed system, and air
is prefilled in the container to facilitate drainage. The container does not
require entry of external air during administration.
The container has two ports: one is the administration outlet port for attachment
of an intravenous administration set and the other port has a medication site
for addition of supplemental medication (See Directions
for Use). The primary function of the overwrap is to protect the container
from the physical environment.Last reviewed on RxList: 4/20/2009




Normal Saline Drug Description
SODIUM CHLORIDE
(sodium chloride) Injection
DRUG DESCRIPTION
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid
and electrolyte replenishment in single dose containers for intravenous administration.
It contains no antimicrobial agents. The nominal pH is 5.5 (4.5 to 7.0). Composition,
osmolarity, and ionic concentration are shown below:
0.45% Sodium Chloride Injection, USP contains 4.5 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 154 mOsmol/L (calc). It contains 77 mEq/L sodium
and 77 mEq/L chloride.
0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride,
USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L
sodium and 154 mEq/L chloride.
The flexible container is made with non-latex plastic materials specially designed
for a wide range of parenteral drugs including those requiring delivery in containers
made of polyolefins or polypropylene. For example, the AVIVA container system
is compatible with and appropriate for use in the admixture and administration
of paclitaxel. In addition, the AVIVA container system is compatible with and
appropriate for use in the admixture and administration of all drugs deemed
compatible with existing polyvinyl chloride container systems. The solution
contact materials do not contain PVC, DEHP, or other plasticizers.
The suitability of the container materials has been established through biological
evaluations, which have shown the container passes Class VI U.S. Pharmacopeia
(USP) testing for plastic containers. These tests confirm the biological safety
of the container system. The flexible container is a closed system, and air
is prefilled in the container to facilitate drainage. The container does not
require entry of external air during administration.
The container has two ports: one is the administration outlet port for attachment
of an intravenous administration set and the other port has a medication site
for addition of supplemental medication (See Directions
for Use). The primary function of the overwrap is to protect the container
from the physical environment.Last reviewed on RxList: 4/20/2009





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Your doctor has ordered sodium chloride flush to be used to keep your intravenous (IV) catheter from becoming blocked and to remove any medicine from the IV catheter site. Sodium Chloride (Catheter Flush) Injection: MedlinePlus Drug ...


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