0.9% SODIUM CHLORIDE INJECTION
- Manufacturer
- Baxter Healthcare Corporation | Baxter Healthcare (Shanghai) Co. Ltd.
- Effective date
- 2025-01-24
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 21:24:26
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
HEALTH CARE PROFESSIONAL LETTER



Reporting Adverse Events or Product Quality Issues
To report adverse events associated with these imported products, please call Baxter at 1-866-888-2472, or fax: 1- 800-759-1801. Adverse events or quality problems experienced with the use of these imported products may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax:
• Complete and submit the report Online:
www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program
• Regular mail or Fax: Download form
www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
To report product quality issues associated with these imported products, please contact Baxter Product Surveillance through Baxter - Product Feedback Portal (
productfeedback.baxter.com/%22%20/o%20%22https:/productfeedback.baxter.com/%22%20/t%20%22_blank).
Please also refer to the local prescribing information of the imported product, translated into English, available for:
• 0.9% Sodium Chloride Injection (click
nctr-crs.fda.gov/fdalabel/ui/spl-summaries/criteria/723233)
• 5% Glucose Injection (click
nctr-crs.fda.gov/fdalabel/ui/spl-summaries/criteria/723235)
• 10% Glucose Injection (click
nctr-crs.fda.gov/fdalabel/ui/spl-summaries/criteria/723237)
• 5% Glucose/0.9% Sodium Chloride Injection (click
nctr-crs.fda.gov/fdalabel/ui/spl-summaries/criteria/723238)
Please refer to the FDA-approved prescribing information for each drug product listed below:
• 0.9% Sodium Chloride Injection USP (click
www.dailymed.nlm.nih.gov/dailymed/getFile.cfm?setid=f55bd888-5e01-474d-871b-24654c070178&type=pdf&name=f55bd888-5e01-474d-871b-24654c070178)
• 5% Dextrose Injection USP (click
www.dailymed.nlm.nih.gov/dailymed/getFile.cfm?setid=3bb406a9-f5cb-403a-b1bb-5c4facbea3d5&type=pdf&name=3bb406a9-f5cb-403a-b1bb-5c4facbea3d5)
• 10% Dextrose Injection USP (click
www.dailymed.nlm.nih.gov/dailymed/getFile.cfm?setid=3bb406a9-f5cb-403a-b1bb-5c4facbea3d5&type=pdf&name=3bb406a9-f5cb-403a-b1bb-5c4facbea3d5)
• 5% Dextrose/0.9% Sodium Chloride Injection USP (click
www.accessdata.fda.gov/drugsatfda_docs/label/2019/016678s007,016683s103,016687s104,016689s107,016697s098lbl.pdf)








PACKAGE INSERT
PACKAGE/LABEL PRINCIPAL DISPLAY PANEL


Baxter Logo Trademark
A6C1322US
SODIUM CHLORIDE INJECTION
50
100
150
200
250ml
0.9% Sodium Chloride
[Strength] 250ml: 2.25g
[Description] This product is a clear, colorless liquid
[Dosage and Administration] Intravenous drip See the package
insert for details
For details of [Indications], [Adverse Reactions],
[Contraindications], and [Precautions], please refer to the
package insert
[Storage] Store in overwrap
The solution should be clear and should be used
up at one time
Inspect the inner bag by squeezing it and discard
solution if leakage occurs
License Number: H19994066
AA
[Drug Marketing Authorization Holder] [Manufacturer]
Name: Baxter Healthcare (Shanghai) Co., Ltd.
Address: No. 388, Tingzhu Road, Jinshan District, Shanghai
Barcode
(01)00303389791010
LOT
MFG
EXP
0.9% Sodium Chloride Injection
250ml X 40
LOT S0000000 EXP YYYY-MM
A6C1322US 1C/N LIC H19994066
0.9% Sodium Chloride Injection
250ml X 40
LOT S0000000 EXP YYYY-MM
MFG YYYY-MM-DD 1C/N 0000


Baxter Logo Trademark
A6C1323US
SODIUM CHLORIDE INJECTION
100
200
300
400
500ml
0.9% Sodium Chloride
[Strength] 500ml: 4.5g
[Description] This product is a clear, colorless liquid
[Dosage and Administration] Intravenous drip See the package
insert for details
For details of [Indications], [Adverse Reactions],
[Contraindications], and [Precautions], please refer to the
package insert
[Storage] Store in overwrap
The solution should be clear and should be used
up at one time
Inspect the inner bag by squeezing it and discard
solution if leakage occurs
License Number: H19983148
AA
[Drug Marketing Authorization Holder] [Manufacturer]
Name: Baxter Healthcare (Shanghai) Co., Ltd.
Address: No. 388, Tingzhu Road, Jinshan District, Shanghai
Barcode
(01)00303389808015
LOT
MFG
EXP
0.9% Sodium Chloride Injection
500ml X 24
LOT S0000000 EXP YYYY-MM
A6C1323US 1C/N LIC H19983148
0.9% Sodium Chloride Injection
500ml X 24
LOT S0000000 EXP YYYY-MM
MFG YYYY-MM-DD 1C/N 0000


Baxter Logo Trademark
A6C1324US
SODIUM CHLORIDE INJECTION
100
200
300
400
500
600
700
800
900
1000ml
0.9% Sodium Chloride
[Strength] 1000ml: 9g
[Description] This product is a clear, colorless liquid
[Dosage and Administration] Intravenous drip See the package
insert for details
For details of [Indications], [Adverse Reactions],
[Contraindications], and [Precautions], please refer to the
package insert
[Storage] Store in overwrap
The solution should be clear and should be used
up at one time
Inspect the inner bag by squeezing it and discard
solution if leakage occurs
License Number: H19983149
AA
[Drug Marketing Authorization Holder] [Manufacturer]
Name: Baxter Healthcare (Shanghai) Co., Ltd.
Address: No. 388, Tingzhu Road, Jinshan District, Shanghai
Barcode
(01)00303389793014
LOT
MFG
EXP
0.9% Sodium Chloride Injection
1000ml X 12
LOT S0000000 EXP YYYY-MM
A6C1324US 1C/N LIC H19983149
0.9% Sodium Chloride Injection
1000ml X 12
LOT S0000000 EXP YYYY-MM
MFG YYYY-MM-DD 1C/N 0000
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1807639 | sodium chloride 0.9 % in 1000 ML Injection | PSN | 4 |
| 1807633 | sodium chloride 0.9 % in 250 ML Injection | PSN | 4 |
| 1807634 | sodium chloride 0.9 % in 500 ML Injection | PSN | 4 |
| 1807639 | 1000 ML sodium chloride 9 MG/ML Injection | SCD | 4 |
| 1807633 | 250 ML sodium chloride 9 MG/ML Injection | SCD | 4 |
| 1807634 | 500 ML sodium chloride 9 MG/ML Injection | SCD | 4 |
| 1807639 | 1000 ML NaCl 9 MG/ML Injection | SY | 4 |
| 1807633 | 250 ML NaCl 9 MG/ML Injection | SY | 4 |
| 1807634 | 500 ML NaCl 9 MG/ML Injection | SY | 4 |
| 1807639 | sodium chloride 0.9 % per 1000 ML Injection | SY | 4 |
| 1807633 | sodium chloride 0.9 % per 250 ML Injection | SY | 4 |
| 1807634 | sodium chloride 0.9 % per 500 ML Injection | SY | 4 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0338-9791-01 | Sodium Chloride | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | 4 | |
| 0338-9791-40 | Sodium Chloride | 40 in 1 CARTON | INJECTION, SOLUTION | 40 | 4 | |
| 0338-9793-01 | Sodium Chloride | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | 4 | |
| 0338-9793-12 | Sodium Chloride | 12 in 1 CARTON | INJECTION, SOLUTION | 12 | 4 | |
| 0338-9808-01 | Sodium Chloride | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | 4 | |
| 0338-9808-24 | Sodium Chloride | 24 in 1 CARTON | INJECTION, SOLUTION | 24 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0338-9791 | SODIUM CHLORIDE INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 4 | Current NDC, 2 package rows | 20250130_93aeac13-41de-4452-9f38-d6b4f38ada30.zip |
| 0338-9793 | SODIUM CHLORIDE INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 4 | Current NDC, 2 package rows | 20250130_93aeac13-41de-4452-9f38-d6b4f38ada30.zip |
| 0338-9808 | SODIUM CHLORIDE INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 4 | Current NDC, 2 package rows | 20250130_93aeac13-41de-4452-9f38-d6b4f38ada30.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0338-9791-01 | ML - Milliliter | 0338-9791 | 53c9df97-584a-40d9-a19d-0a046056df89 | 1 | 2025-02-10 |
| 0338-9791-40 | ML - Milliliter | 0338-9791 | e86f7cf2-5ea0-4158-9c58-05e07e9e9ee1 | 1 | 2025-02-10 |
| 0338-9793-01 | ML - Milliliter | 0338-9793 | cd9ab20b-d3b1-4579-bab4-2a8f977fed8e | 1 | 2025-02-10 |
| 0338-9793-12 | ML - Milliliter | 0338-9793 | c7399cb0-9a25-42b8-9974-df0cc30eb084 | 1 | 2025-02-10 |
| 0338-9808-01 | ML - Milliliter | 0338-9808 | a7e7fd99-1b4b-44db-8b12-f18aac454272 | 1 | 2025-02-10 |
| 0338-9808-24 | ML - Milliliter | 0338-9808 | d6c08314-f27f-47c5-af3f-e5548bba539b | 1 | 2025-02-10 |
Products#
Every source-derived product name is available through these pages.
- Sodium Chloride
- SODIUM CATION
- CHLORIDE ION
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0338-9791 | 0338-9791-01, 0338-9791-40 |
| 0338-9793 | 0338-9793-01, 0338-9793-12 |
| 0338-9808 | 0338-9808-01, 0338-9808-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| WATER | 059QF0KO0R | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 93aeac13-41de-4452-9f38-d6b4f38ada30 | 2025-01-24 | 0338-9793-12 0338-9791-01 0338-9808-24 0338-9791-40 0338-9808-01 0338-9793-01 0338-9793 0338-9791 0338-9808 00338979312 00338980824 00338979301 00338979140 00338979101 00338980801 db478972-6e08-47d1-841c-92b4051a0527 93aeac13-41de-4452-9f38-d6b4f38ada30 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.







