Label: SODIUM CHLORIDE NORMAL SALT- sodium chloride tablet

  • NDC Code(s): 58657-118-01
  • Packager: Method Pharmaceuticals
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 10, 2023

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  • 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
  • Indication

    Electrolyte Replenisher

  • Ask a physician

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

  • Stop use

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

  • If pregnant or breastfeeding,

    ask a health professional before use.

  • Keep out of reach of children

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

  • Directions

    • 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

    Do not use without consulting a physician.

  • Active ingredients

    Sodium Chloride

  • Inactive Ingredient

    NONE

  • Sodium Chloride

    label

  • INGREDIENTS AND APPEARANCE
    SODIUM CHLORIDE  NORMAL SALT
    sodium chloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58657-118
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE1 g
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize12mm
    FlavorImprint Code M118
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58657-118-01100 in 1 BOTTLE; Type 0: Not a Combination Product09/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01809/23/2021
    Labeler - Method Pharmaceuticals (060216698)
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