0.9 % Sodium Chloride Injection, USP

SODIUM CHLORIDE by

Drug Labeling and Warnings

SODIUM CHLORIDE by is a Prescription medication manufactured, distributed, or labeled by Baxter Healthcare Corporation, Baxter Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SODIUM CHLORIDE- sodium chloride injection 
Baxter Healthcare 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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0.9 % Sodium Chloride Injection, USP

HEALTH CARE PROVIDER LETTER

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PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

Sodium Chloride JB0042 Representative Container Label

Container Label

JB0042
Mini-Bag Plus
50 mL

0.9% Sodium Chloride Injection USP

DIN 00060208

APPROX mmol/L Na -154 Cl - 154 mOsmol/L 308 pH 5.5
SINGLE DOSE / DOSAGE UNIQUE

PER/PAR 100 mL SODIUM CHLORIDE USP/CHLORURE DE
SODIUM USP - 900 mg pH MAY BE ADJUSTED WITH SODIUM
HYDROXIDE / IV FLUID AND ELECTROLYTE REPLENISHER /
PRESCRIBING INFORMATION AVAILABLE UPON REQUEST /
MUST NOT BE USED IN SERIES CONNECTIONS / SQUEEZE
AND INSPECT BAG / DISCARD IF LEAKING / STORE AT 15°C TO
25°C

Barcode (01)00809080000968

pH PEUT ETRE AJUSTE AVEC DE L’HYDROXYDE DE SODIUM /
SOLUTION IV AVEC ELECTROLYTES / INFORMATION PO-
SOLOGIQUE DISPONIBLE SUR DEMANDE / NE DOIT PAS ETRE
MONTE EN SERIE / PRESSER ET INSPECTER LE SAC / JETER
EN CAS DE FUITES / GARDER ENTRE 15 °C ET 25 °C

NONPYROGENIC / STERILE / APYROGENE
Viaflex® PVC CONTAINER / CONTENANT DE PVC

ACTIVATE BEFORE USE
ACTIVER AVANT D’UTILISER

Baxter Logo
Baxter Corporation
Mississauga ON L5N 0C2

No LATEX Logo
88-70-20-407

Sodium Chloride JB0043 Representative Container Label

Container Label

JB0043
Mini-Bag Plus
100 mL

0.9% Sodium Chloride Injection USP

DIN 00060208

APPROX mmol/L Na -154 Cl - 154 mOsmol/L 308
pH 5.5
SINGLE DOSE / DOSAGE UNIQUE

PER/PAR 100 mL SODIUM CHLORIDE USP/CHLORURE
DE SODIUM USP - 900 mg pH MAY BE ADJUSTED
WITH SODIUM HYDROXIDE / IV FLUID AND ELECTRO-
LYTE REPLENISHER / PRESCRIBING INFORMATION
AVAILABLE UPON REQUEST / MUST NOT BE USED
IN SERIES CONNECTIONS / SQUEEZE AND INSPECT
BAG / DISCARD IF LEAKING / STORE AT 15°C TO 25°C

Barcode (01)00809080000975

pH PEUT ETRE AJUSTE AVEC DE L’HYDROXYDE DE SODIUM / SOLU-
TION IV AVEC ELECTROLYTES / INFORMATION POSOLOGIQUE DISPONI-
BLE SUR DEMANDE / NE DOIT PAS ETRE MONTE EN SERIE / PRESSER
ET INSPECTER LE SAC / JETER EN CAS DE FUITES /
GARDER ENTRE 15 °C ET 25 °C

NONPYROGENIC / STERILE / APYROGENE
Viaflex® PVC CONTAINER / CONTENANT DE PVC

ACTIVATE BEFORE USE
ACTIVER AVANT D’UTILISER

No LATEX Logo
88-70-20-408

Baxter Logo
Baxter Corporation
Mississauga ON L5N 0C2

SODIUM CHLORIDE 
sodium chloride injection
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-9531
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE900 mg  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0338-9531-9696 in 1 CARTON10/13/201710/13/2017
150 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug for use in drug shortage10/13/201710/13/2017
SODIUM CHLORIDE 
sodium chloride injection
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-9535
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE900 mg  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0338-9535-7272 in 1 CARTON10/13/201710/13/2017
1100 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug for use in drug shortage10/13/201710/13/2017
Labeler - Baxter Healthcare Corporation (005083209)
Establishment
NameAddressID/FEIBusiness Operations
Baxter Corporation205087968ANALYSIS(0338-9531, 0338-9535) , LABEL(0338-9531, 0338-9535) , MANUFACTURE(0338-9531, 0338-9535) , PACK(0338-9531, 0338-9535) , STERILIZE(0338-9531, 0338-9535)

Revised: 11/2019
 
Baxter Healthcare Corporation