Over-the-counter drug · OTC MONOGRAPH DRUG

Sodium Chloride NDC 57237-361

Sodium chloride 1000 mg/1 · Tablet · Oral · Rising Pharma Holdings, Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)57237-361Labeler and product segments. Claims need a package NDC.
Product NDC at billing width57237-0361Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
57237-361-0157237036101100 TABLET in 1 BOTTLE (57237-361-01)Marketed from Nov 6, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Sodium Chloride
Generic name (nonproprietary)
sodium chloride
Active ingredients
Sodium chloride — 1000 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Rising Pharma Holdings, Inc.NDC labeler code 57237
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 018
Marketing start
Listing expires
Identifiers
Product ID 57237-361_7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8SPL ID 7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8SPL set ID 42870188-b1d7-4934-a6c0-310530497dacRxCUI 313009UNII 451W47IQ8X

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N457237036101 followed by a unit qualifier and the quantity

Package 57237-0361-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses: for the preparation of normal isotonic solution of sodium chloride as an electrolyte replenisher for the prevention of heat cramps due to excessive perspiration any alternative use as directed by a physician

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 57237-361

What is NDC 57237-361?
57237-361 is the product NDC for Sodium Chloride, Sodium chloride 1000 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium Chloride.
What is the active ingredient?
Sodium chloride.
Who is the labeler?
Rising Pharma Holdings, Inc., NDC labeler code 57237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sodium Chloride?
116 other product NDCs are listed under this name. See all Sodium Chloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sodium Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium ChlorideSodium chloride 50 mg/gOintmentOphthalmicYYBA CORP73581-70773581-0707-0173581-0707-03
Sodium ChlorideSodium chloride 1 g/1TabletOralMethod Pharmaceuticals, LLC58657-11958657-0119-01
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50265219-0502-10
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50465219-0504-20
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationBecton Dickinson and Company17271-80017271-0800-0717271-0800-0817271-0800-09
Sodium chlorideSodium chloride .9 g/100mLInjection, SolutionIrrigationFresenius Kabi USA, LLC65219-50665219-0506-30
Sodium Chloridesodium chloride tabletsSodium chloride 1000 mg/1TabletOralKesin Pharma Corporation81033-02881033-0028-01
Sodium Chloridesodium chloride tabletSodium chloride 1000 mg/1TabletOralBelleview Bioscience LLC84447-00284447-0002-01
Sodium ChlorideSodium chloride 900 mg/100mLIrrigantIrrigationBaxter Healthcare Company0338-983400338-9834-04
Sodium ChlorideSodium chloride 900 mg/100mLIrrigantIrrigationBaxter Healthcare Company0338-011000338-0110-04

All 117 Sodium Chloride NDCs

Other NDCs under M 018

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 018
ProductStrengthForm · routeLabelerProduct NDC
Medi-First Lubricant Eye Dropscarboxymethylcellulose sodiumCarboxymethylcellulose sodium, Unspecified form .5 g/100mLSolutionOphthalmicUnifirst First Aid Corporation47682-193
Signature Care Eye Drops High Performancepolyethylene glycol 400, propylene glycolPolyethylene glycol 400 .4 g/100mL; Propylene glycol .3 g/100mLSolution/ dropsOphthalmicBetter Living Brands LLC21130-702
Walgreens Lubricant Eye Drops High Performance 15mL and twin packpolyethylene glycol 400, propylene glycolPropylene glycol .3 g/100mL; Polyethylene glycol 400 .4 g/100mLSolution/ dropsOphthalmicWalgreen Company0363-4549
Plus Rinse Emergency Eyewashpurified waterWater 99.1 mL/100mLLiquidOphthalmicINNOVATIVE SAFETY SUPPLY INC.72598-022
Sunmark Lubricant Eye Dropspolypropylene glycol 400, propylene glycolPolyethylene glycol 400 .4 g/100mL; Propylene glycol .3 g/100mLSolution/ dropsOphthalmicStrategic Sourcing Services LLC49348-947
Refresh Digitalcarboxymethylcellulose sodium, glycerin, polysorbate 80Carboxymethylcellulose sodium 5 mg/mL + 2 more ingredientsSolution/ dropsOphthalmicAllergan, Inc.0023-6952
Sodium Chloride Hypertonicity Ophthalmic Solution, 5%Sodium chloride 50 mg/mLSolution/ dropsOphthalmicReliable 1 Laboritories LLC69618-077
Walgreens Sterile Soothing Eye Washpurified waterWater 99.05 mL/100mLLiquidOphthalmicWalgreens0363-0700
Sodium Hyaluronate Eye Dropssodium hyaluronateSodium hyaluronate .1 g/100gLiquidOphthalmicGuangzhou Hechuang Commercial Service Co.,Ltd.87298-037
Retaine CMCcarboxymethylcellulose sodiumCarboxymethylcellulose sodium, Unspecified 5 mg/mLSolution/ dropsOphthalmicOCuSOFT LLC54799-460
Equate Lubricant Eye Dropscarboxymethylcellulose sodium, glycerinCarboxymethylcellulose sodium .5 g/100mL; Glycerin .9 g/100mLSolution/ dropsOphthalmicWalmart79903-365
Equate Redness and Dry Eye Reliefglycerin, naphazoline hydrochlorideGlycerin .25 g/100mL; Naphazoline hydrochloride .012 g/100mLSolutionOphthalmicWalmart79903-362
Original Redness Relievertetrahydrolizine hclTetrahydrozoline hydrochloride .05 g/100mLSolution/ dropsOphthalmicWalmart79903-363
REFRESH Optive Mega-3carboxymethylcellulose sodium, glycerin and polysorbate 80Carboxymethylcellulose sodium 5 mg/mL + 2 more ingredientsSolution/ dropsOphthalmicAllergan, Inc.0023-4230
Best Choice Artificial Tearspolyvinyl alcohol, povidonePolyvinyl alcohol .5 g/100mL; Povidone .6 g/100mLSolution/ dropsOphthalmicBest Choice63941-015
Dry Eye Reliefcarboxymethylcellulose sodiumCarboxymethylcellulose sodium, Unspecified 10 mg/mLGelOphthalmicCARDINAL HEALTH 110, LLC. DBA LEADER70000-0089
Equate Lubricant Eye Dropscarboxymethylcellulose sodiumCarboxymethylcellulose sodium .5 mg/100mLSolution/ dropsOphthalmicWalmart79903-364
Lubricant Dropscarboxymethylcellulose sodiumCarboxymethylcellulose sodium, Unspecified 5 mg/mLSolution/ dropsOphthalmicCARDINAL HEALTH 110, LLC. DBA LEADER70000-0090
Sodium Chloride Hypertonicity Ophthalmicsodium chlorideSodium chloride 50 mg/gOintmentOphthalmicRugby Laboratories0536-1253
Meijer Redness Relieftetrahydrozoline hciTetrahydrozoline hydrochloride .05 g/100mLSolution/ dropsOphthalmicMeijer Distribution, Inc.41250-814

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