Sodium Chloride Injection, solution by HK INNO.N CORPORATION

Sodium Chloride Injection, solution by

Drug Labeling and Warnings

Sodium Chloride Injection, solution by is a Prescription medication manufactured, distributed, or labeled by HK INNO.N CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SODIUM CHLORIDE INJECTION, SOLUTION- sodium chloride injection injection 
HK INNO.N CORPORATION

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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INDICATIONS & USAGE

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

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

English Package Label

Inno,N Box Images

SODIUM CHLORIDE INJECTION, SOLUTION 
sodium chloride injection injection

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 84988-1440
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	9 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84988-1440-1	1000 mL in 1 BAG; Type 0: Not a Combination Product	11/26/2024	02/12/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug for use in drug shortage		11/26/2024	02/12/2026

Labeler - HK INNO.N CORPORATION (689049556)

Registrant - HK INNO.N CORPORATION (689049556)

Establishment
Name	Address	ID/FEI	Business Operations
HK INNO.N CORPORATION		689049556	manufacture(84988-1440)

Revised: 12/2025

Document Id: 4501a796-1db0-c65d-e063-6294a90a5f01

34391-3

Set id: 27c3175d-5df4-dc92-e063-6394a90ab5f4

Version: 4

Effective Time: 20251202