0.9% Sodium Chloride Injection, USP

Manufacturer
Hikma Pharmaceuticals USA Inc.
Effective date
2019-12-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 20:31:13

Label at a glance#

ProductSodium Chloride
Active ingredientSODIUM CHLORIDE
Label structure11 sections

Indications and uses

This parenteral preparation indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered. 

Dosage and administration

The volume of the preparation to be used for diluting or dissolving any drug for injection is dependent on the vehicle concentration, dose and route of administration as recommended by the manufacturer. Use aseptic technique for entry and withdrawal from container. This parenteral should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. ...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rx only 

DESCRIPTION

DESCRIPTION SECTION

This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection.

0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. Its chloride and sodium ion concentrations are approximately 0.154 mEq of each per milliliter and its calculated osmolality is 0.308 milliosmols per mL. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment, pH 5.3 (4.5 to 7.0).

Sodium chloride, USP occurs as colorless cubic crystals or white crystalline powder and has a saline taste. Sodium chloride is freely soluble in water. The empirical formula for sodium chloride is NaCl, and the molecular weight is 58.44.

The ampul is a colorless sealed sterile glass container.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Sodium chloride in water dissociates to provide sodium (Na+) and chloride (Cl–) ions. These ions are normal constituents of the body fluids (principally extracellular) and are essential for maintaining electrolyte balance.

The distribution and excretion of sodium (Na+) and chloride (Cl–) are largely under the control of the kidney which maintains a balance between intake and output.

The small volume of fluid and amount of sodium chloride provided by 0.9% Sodium Chloride Injection, USP when used only as an isotonic vehicle for parenteral injection of drugs, is unlikely to exert a significant effect on fluid and electrolyte balance except possibly in neonates and very small infants.

Water is an essential constituent of all body tissues and accounts for approximately 70% of total body weight. Average normal adult daily requirement ranges from two to three liters (1 to 1.5 liters each for insensible water loss by perspiration and urine production).

Water balance is maintained by various regulatory mechanisms. Water distribution depends primarily on the concentration of electrolytes in the body compartments and sodium (Na+) plays a major role in maintaining physiologic equilibrium.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

This parenteral preparation indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered. 

PRECAUTIONS

PRECAUTIONS SECTION

General

GENERAL PRECAUTIONS SECTION

Consult the manufacturer’s instructions for choice of vehicle, appropriate dilution or volume for dissolving the drugs to be injected, including the route and rate of injection.

Inspect reconstituted (diluted or dissolved) drugs for clarity (if soluble) and freedom from unexpected precipitation or discoloration prior to administration. 

Pregnancy

PREGNANCY SECTION

PREGNANCY CATEGORY C

SPL UNCLASSIFIED SECTION

Animal reproduction studies have not been conducted with 0.9% Sodium Chloride Injection, USP. It is also not known whether sodium chloride injection containing additives can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sodium chloride injection containing additives should be given to a pregnant woman only if clearly needed.

Pediatric Use

PEDIATRIC USE SECTION

The safety and effectiveness in the pediatric population are based on the similarity of the clinical conditions of the pediatric and adult populations. In neonates or very small infants the volume of fluid may affect fluid and electrolyte balance. 

Drug Interactions

DRUG INTERACTIONS SECTION

Some drugs for injection may be incompatible in a given vehicle, or when combined in the same vehicle or in a vehicle containing benzyl alcohol.

Consult with pharmacist, if available.

Use aseptic technique for entry and withdrawal from all containers.

When diluting or dissolving drugs, mix thoroughly and use promptly.

Do not store reconstituted solutions of drugs for injection unless otherwise directed by the manufacturer of the solute.

Do not use unless the solution is clear and seal intact. Do not reuse single-dose containers, discard unused portion. 

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Reactions which may occur because of this solution, added drugs or the technique of reconstitution or administration include febrile response, local tenderness, abscess, tissue necrosis or infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection and extravasation.

If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate countermeasures, and if possible, retrieve and save the remainder of the unused vehicle for examination.

OVERDOSAGE

OVERDOSAGE SECTION

Use only as a diluent or solvent. This parenteral preparation is unlikely to pose a threat of carbohydrate, sodium chloride or fluid overload except possibly in neonates or very small infants. In the event these should occur, re-evaluate the patient and institute appropriate corrective measures. See PRECAUTIONS and ADVERSE REACTIONS. 

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

The volume of the preparation to be used for diluting or dissolving any drug for injection is dependent on the vehicle concentration, dose and route of administration as recommended by the manufacturer.

Use aseptic technique for entry and withdrawal from container.

This parenteral should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. See PRECAUTIONS.

HOW SUPPLIED

HOW SUPPLIED SECTION

0.9% Sodium Chloride Injection, USP, is supplied in the following:

10 mL ampuls packaged in 100s (NDC 0641-1512-36) 

Storage

SPL UNCLASSIFIED SECTION

Store at 20° - 25°C (68°-77°F), excursions permitted to 15° - 30°C (59° - 86°F) [See USP Controlled Room Temperature]. Avoid freezing. 

SPL UNCLASSIFIED SECTION

To report SUSPECTED ADVERSE REACTIONS, contact West-Ward Pharmaceutical Corp. at 1-877-845-0689, or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

For Product Inquiry call 1-877-845-0689.

Manufactured by:

West-Ward logo
West-Ward logo

WEST-WARD
PHARMACEUTICALS
Eatontown, NJ 07724 USA

November 2011

462-602-00

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0.9% Sodium Chloride Injection, USP
0.308 mOsmol/mL
10 mL Ampul
NDC 0641-1512-10

0.9% Sodium Chloride Injection, USP 0.308 mOsmol/mL 10 mL Ampul0.9% Sodium Chloride Injection, USP 0.308 mOsmol/mL 10 mL Ampul 

0.9% Sodium Chloride Injection, USP
0.308 mOsmol/mL
100 x 10 mL Ampuls
NDC 0641-1512-36

0.9% Sodium Chloride Injection, USP 0.308 mOsmol/mL 100 x 10 mL Ampuls
0.9% Sodium Chloride Injection, USP 0.308 mOsmol/mL 100 x 10 mL Ampuls

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1807637sodium chloride 0.9 % in 10 ML InjectionPSN4
180763710 ML sodium chloride 9 MG/ML InjectionSCD4
180763710 ML NaCl 9 MG/ML InjectionSY4
1807637normal saline 10 mL InjectionSY4
1807637sodium chloride 0.9 % per 10 ML InjectionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
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5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0641-1512-362025-01-30C16284748780-12cef2736-7f72-d83d-e063-dadaa90ab31f0.9% Sodium Chloride Injection, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0641-1512-10Sodium Chloride10 mL in 1 AMPULEINJECTION104
0641-1512-36Sodium Chloride100 in 1 CARTONINJECTION1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0641-1512SODIUM CHLORIDE INJECTION [HIKMA PHARMACEUTICALS USA INC.]4Legacy NDC, 2 package rows20191231_fefc9ea8-a2de-49ab-8d79-d8337248ff0e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X3
CHLORIDE IONACTIVE MOIETYQ32ZN486983
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CB3
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32I3
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0641-15120641-1512-10, 0641-1512-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 6 · 322 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SUSPENSION / INTRAMUSCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IFILM, EXTENDED RELEASE / TRANSDERMAL0.85 mgExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / SUBARACHNOIDADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SUSPENSION / INTRAVITREALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / PERIDURALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INTRAVENOUS1037 mgExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SUSPENSION / INTRAVENOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISUSPENSION, EXTENDED RELEASE / INTRASYNOVIALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / SUBMUCOSALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / EXTRACORPOREALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRAVENOUS78 mgExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRAMUSCULAR78 mgExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION/ DROPS / OPHTHALMICADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSUSPENSION, EXTENDED RELEASE / INTRAMUSCULAR5 mgExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISYRUP / ORAL71 mg/5mlExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / INTRADERMALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INTRAMUSCULAR1037 mgExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / RESPIRATORY (INHALATION)ADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ILOTION / TOPICAL21 mgExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / ORAL9120 mgExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRA-ARTERIALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, EMULSION / INTRAVENOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISUSPENSION, EXTENDED RELEASE / SUBCUTANEOUSNAExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRAVITREALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRA-AMNIOTICADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRA-ARTERIAL176 mgExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRATUMORADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRAVENOUS456 mgExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRASPINALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION, CONCENTRATE / INTRAVENOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBAEROSOL, SPRAY / RESPIRATORY (INHALATION)1.5 %w/wExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IJELLY / TOPICALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / AURICULAR (OTIC)0.8 %w/wExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICREAM, AUGMENTED / TOPICAL6 mgExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / ORAL223 mgExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / URETHRALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ITABLET, COATED / ORALNAExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / INTRAVASCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSUSPENSION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRACAVITARYADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSUSPENSION / OPHTHALMICADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ILIQUID / INTRAVENOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISPRAY, METERED / NASALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / SUBCONJUNCTIVALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / PARENTERALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBAEROSOL, METERED / RESPIRATORY (INHALATION)0.7 %w/wExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICONCENTRATE / ORAL10 mg/5mlExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INFILTRATIONADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISUSPENSION, EXTENDED RELEASE / INTRA-ARTICULARADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRAPLEURALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / AURICULAR (OTIC)0.37 %w/vExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBTABLET, EXTENDED RELEASE / ORAL24 mgExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRACAUDALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / SUBMUCOSALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / INTRAPERITONEALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRA-ARTICULARADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS0.18 %w/vExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / EXTRACORPOREALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / IRRIGATIONADJ PHExact identifier — unii candidate
148 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A201850-001SODIUM CHLORIDE 0.9%SODIUM CHLORIDE90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-2084e616aacf4f…
2026-08-18 06:07:402026-07A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-2031067a03dcf5…
2025-08-23 18:47 UTC2025-08A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-206a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-2003ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-202680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-205bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-2079d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-20301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-201e350fbaab3a…
2024-05-31 18:47 UTC2024-05A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTION2012-01-208072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-205c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-205d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-204b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-2074a2ff9319b5…
2022-03-09 01:35 UTC2022-03A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-2087673890dc5c…
2021-03-12 10:30 UTC2021-03A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-205aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-208869cabd3fbd…
2020-11-12 02:37 UTC2020-11A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20c0c555d07b60…
2019-12-14 00:12 UTC2019-12A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-203f01610625f2…
2019-09-15 20:21 UTC2019-09A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20b00525d2431f…
2019-07-19 19:46 UTC2019-07A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-206a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-201c564ffb4f44…
2023-12-20 04:57 UTC2023-12A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-20ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-20a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-209b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A201850-001SODIUM CHLORIDE 0.9%90MG/10ML (9MG/ML)SOLUTION / INJECTIONAP2012-01-20a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-203f0d92c62455…
2023-05-13 08:27 UTC2023-05A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20053a50430f4f…
2023-01-26 05:58 UTC2023-01A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-203bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-203a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A201850-001SODIUM CHLORIDE 0.9%9MG/MLINJECTABLE / INJECTIONAP2012-01-20f41ea6bd6efb…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A201850-001AP15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A201850-001AP15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A201850-001AP14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A201850-001AP174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A201850-001AP1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A201850-001AP1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A201850-001AP187673890dc5c…
2021-03-12 10:30 UTC2021-03A201850-001AP15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A201850-001AP18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A201850-001AP1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A201850-001AP13f01610625f2…
2019-09-15 20:21 UTC2019-09A201850-001AP1b00525d2431f…
2019-07-19 19:46 UTC2019-07A201850-001AP1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A201850-001AP16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A201850-001AP11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A201850-001AP1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A201850-001AP1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A201850-001AP19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A201850-001AP1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A201850-001AP13f0d92c62455…
2023-05-13 08:27 UTC2023-05A201850-001AP1053a50430f4f…
2023-01-26 05:58 UTC2023-01A201850-001AP13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A201850-001AP13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A201850-001AP1f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A201850-001AP1e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07A201850-001AP1cb3db0bc1861…

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
90d2e8c2-7688-4a7d-9a1c-009f4a7e159cfefc9ea8-a2de-49ab-8d79-d8337248ff0e2019-12-30Adverse reactionsExact identifier
spl id: 90d2e8c2-7688-4a7d-9a1c-009f4a7e159c
spl set id: fefc9ea8-a2de-49ab-8d79-d8337248ff0e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.