FDA.reportPublic FDA data

Sodium Chloride Injection, solution

Manufacturer
HK INNO.N CORPORATION
Effective date
2025-12-02
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:47:26

Label at a glance#

ProductSodium Chloride Injection, solution
Active ingredientSODIUM CHLORIDE
Label structure5 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Sodium Chloride Injection, USP is indicated as a source of water and electrolytes. 0.9% Sodium Chloride Injection, USP is also indicated for use as a priming solution in hemodialysis procedures.

Storage: Store at room temperature 20°C/68°F. to 25°C/77°F.

Medication Administration: Contains medication port and administration port; Twist off shield, left side

These highlights do not include all the information needed to use Sodium Chloride 0.9% Injection. See full prescribing information for Chloride 0.9% Injection. This product is an unapproved product for use in urgent drug shortage” (code C101533).

INSTRUCTIONS FOR USE Contains medication port and administration port; Twist off shield, left side

INSTRUCTIONS FOR USE SECTION

Korean Package LabelKorean Package Label

DHCPLetter for unapproved product for use in urgent drug shortage” (code C101533)

HEALTH CARE PROVIDER LETTER SECTION

SLI - HK Inno DHCPSLI - HK Inno DHCP

English Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

English Package LabelEnglish Package Label

Inno,N Box Images

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package ImagePackage Image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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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
84988-144084988-1440-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

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
4501a796-1db0-c65d-e063-6294a90a5f0127c3175d-5df4-dc92-e063-6394a90ab5f42025-12-02Exact identifier
spl id: 4501a796-1db0-c65d-e063-6294a90a5f01
spl set id: 27c3175d-5df4-dc92-e063-6394a90ab5f4

Reported adverse events (FAERS/openFDA)#

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