Sodium Chloride

Manufacturer
Method Pharmaceuticals
Effective date
2025-10-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:41:34

Label at a glance#

ProductSodium Chloride Normal Salt
Active ingredientSODIUM CHLORIDE
Label structure11 sections

Indications and uses

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

Dosage and administration

to make isotonic solutions of sodium chloride, dissolve one tablet in 120 mL (four ounces) of distilled water and use as directed by a physician. if used an electrolyte replinisher for the prevention of heat cramps due to excessive perspiration take one tablet orally as directed by a physician.

Label contents#

Full prescribing information#

Uses

OTC - PURPOSE SECTION

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

Indication

INDICATIONS & USAGE SECTION

Electrolyte Replenisher

Ask a physician

OTC - ASK DOCTOR SECTION

before use if you have a sodium restricted diet due to multiple organ disease

Stop use

OTC - STOP USE SECTION

and ask a physician if symptoms of heat cramps continue for more than 24 hours.

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • to make isotonic solutions of sodium chloride, dissolve one tablet in 120 mL (four ounces) of distilled water and use as directed by a physician.
  • if used an electrolyte replinisher for the prevention of heat cramps due to excessive perspiration take one tablet orally as directed by a physician.

Warnings

WARNINGS SECTION

Do not use without consulting a physician.

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride

Inactive Ingredient

INACTIVE INGREDIENT SECTION

NONE

Sodium Chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sod-chlorsod-chlor

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313009sodium chloride 1 GM Oral TabletPSN6
313009sodium chloride 1000 MG Oral TabletSCD6
313009NaCl 1000 MG Oral TabletSY6
313009sodium chloride 0.124 MEQ/ML Oral SolutionSY6
313009sodium chloride 0.171 MEQ/ML Oral SolutionSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58657-118-01Sodium ChlorideNormal Salt100 in 1 BOTTLETABLET1006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58657-118-01EA - Each58657-118c2dd68bb-a720-40f0-99e3-ebcaa0806c5212022-02-07

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58657-11858657-118-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-11-19full-release2026-06-01 00:38:59

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
Sodium Chloride Normal SaltSODIUM CHLORIDEMethod Pharmaceuticalsce84727a-3677-4bf0-e053-2995a90a3ec82025-10-21WarningsExact identifier
ndc (package): 58657-118-01
ndc (product): 58657-118
ndc11 (package): 58657011801
spl id: 41b6990d-5e10-e82c-e063-6394a90a2bf6
spl set id: ce84727a-3677-4bf0-e053-2995a90a3ec8

Reported adverse events (FAERS/openFDA)#

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