0363-3109-07 : NDC 2026 Code

0363-3109-07 : Magnesium Sulfate Heptahydrate ( Walgreens Foaming Muscle Relief )

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NDC Code : 0363-3109-07 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0363-3109-07",
    "PackageDescription": "210 mL in 1 BOTTLE, PLASTIC (0363-3109-07) ",
    "NDC11Code": "00363-3109-07",
    "ProductNDC": "0363-3109",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Walgreens Foaming Muscle Relief",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Magnesium Sulfate Heptahydrate",
    "DosageFormName": "LIQUID",
    "RouteName": "TOPICAL",
    "StartMarketingDate": "20251217",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
    "ApplicationNumber": null,
    "LabelerName": "Walgreens",
    "SubstanceName": "MAGNESIUM SULFATE HEPTAHYDRATE",
    "StrengthNumber": "6",
    "StrengthUnit": "[hp_X]/210mL",
    "Pharm_Classes": "Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-09-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20251217",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}