SODIUM CHLORIDE- sodium chloride injection, solution 
Hospira, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Preservative-Free
0.9% Sodium Chloride Injection, USP

Rx only

DESCRIPTION

0.9% Sodium Chloride Injection, USP in Carpuject™ sterile cartridge unit (2 mL, 3 mL, and 5 mL fill), is a sterile aqueous isotonic solution of sodium chloride in Water for Injection. The total osmolar concentration of the solution is 0.31 mOsm/mL. Each mL contains 9 mg of sodium chloride.

CLINICAL PHARMACOLOGY

0.9% Sodium Chloride Injection, USP is a sterile aqueous vehicle having approximately the same osmotic pressure and composition as extracellular fluids. It is nonirritating to tissues.

INDICATIONS AND USAGE

For use as a sterile isotonic vehicle for diluting or dissolving compatible parenteral medications.

PRECAUTIONS

If compatibility is in doubt, consult the appropriate specialized literature before mixing with any drug product. Do not administer if a precipitate appears, if solution is cloudy or hazy, or if any other visible change occurs upon mixing.

For single use only. Discard unused solution.

DOSAGE AND ADMINISTRATION

Use in accord with any warnings or precautions appropriate to the medication being administered.

HOW SUPPLIED

NDC No.

Container

Fill

Quantity

0409-1918-32

Carpuject™ with Luer Lock

2 mL fill in 2 mL cartridge

bins of 50

0409-1918-33

Carpuject™ with Luer Lock

3 mL fill in 5 mL cartridge

bins of 25

0409-1918-35

Carpuject™ with Luer Lock

5 mL fill in 5 mL cartridge

bins of 25

Do not use if solution is discolored or contains a precipitate.

Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature].

Do not freeze.

Revised: November, 2009

Printed in USA

EN-2305

Hospira, Inc., Lake Forest, IL 60045 USA

 

RL-0000

label ndc 0409-1918-32

SODIUM CHLORIDE 
sodium chloride injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0409-1918
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE9 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0409-1918-3250 in 1 CONTAINER
12 mL in 1 CARTRIDGE
2NDC:0409-1918-3325 in 1 CONTAINER
23 mL in 1 CARTRIDGE
3NDC:0409-1918-3525 in 1 CONTAINER
35 mL in 1 CARTRIDGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other09/13/2011
Labeler - Hospira, Inc. (141588017)

Revised: 9/2011
 
Hospira, Inc.