Patient information: uses, side effects, how to take - Sodium Chloride Injection 0.9 g/100 mL

Directions for Use of Plastic Container

Caution: Do not use plastic container in series connection.

To Open

Check for minute leaks by squeezing solution container firmly. If leaks are found, discard solution as sterility may be impaired. If supplemental medication is desired, follow directions below before preparing for administration.

NOTE: Before use, perform the following checks:

Inspect each container. Read the label. Ensure solution is the one ordered and is within the expiration date.

Invert container and carefully inspect the solution in good light for cloudiness, haze, or particulate matter. Any container which is suspect should not be used.

Use only if solution is clear and container and seals are intact.

Preparation for Administration

1. Remove plastic protector from sterile set port at bottom of container.
2. Attach administration set. Refer to complete directions accompanying set.

To Add Medication

Warning: Some additives may be incompatible.

To Add Medication Before Solution Administration

1. Prepare medication site by removing the additive port closure. Swab the exposed medication site before puncturing.
2. Using syringe with 18-22 Ga. needle, puncture medication port and inner diaphragm and inject.
3. Squeeze and tap ports while ports are upright and mix solution and medication thoroughly.

To Add Medication During Solution Administration

1. Close clamp on the set.
2. Prepare medication site by removing the additive port closure. Swab the exposed medication site before puncturing.
3. Using syringe with 18-22 Ga. needle of appropriate length (at least 5/8 inch), puncture resealable medication port and inner diaphragm and inject.
4. Remove container from IV pole and/or turn to an upright position.
5. Evacuate both ports by tapping and squeezing them while container is in the upright position.
6. Mix solution and medication thoroughly.
7. Return container to in use position and continue administration.

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: NDA 019635 · View the label on DailyMed

Revision date stated in the text: December 2022

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Sodium Chloride Injection 0.9 g/100 mL

Rx or OTC

Prescription (Rx)?

This drug is available only with a prescription from a licensed healthcare provider.
Rx

Drug class

Osmotic Laxative

Active ingredient

Sodium chloride 0.9 g/100 mL

Dosage form

Injection, solution

Route

Intravenous

Marketing status

listed in the FDA NDC Directory

Company (applicant)

B BRAUN

FDA approval

NDA 019635New Drug Application (NDA) Approved March 9, 1988

Reference listed drug

This is the reference listed drug (RLD) that generics are compared with.

Therapeutic equivalence (TE) code

APCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book).

Manufacturers

19 labelers list this drug on DailyMed

Drug shortage

Being discontinued since December 3, 2025

Recalls

August 19, 2026: Class I recall: Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene
August 17, 2026: Class I recall: Presence of particulate matter: Particulates identified as fiberglass
April 2, 2026: Class II recall: Lack of Assurance of Sterility

Show more recalls (2)+

March 11, 2026: Class II recall: Lack of Assurance of Sterility
March 11, 2026: Class II recall: Lack of Assurance of Sterility

Packages (NDC)

Package
0.9 g/100 mL – 1000 ml in 1 container / 12 in 1 case NDC 0264-7800-09

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.

Sodium Chloride Injection 0.9 g/100 mL: Uses, Side Effects and Dosage