Maxidol Liquid Gels 20s

GTIN 00056500363008DIN 02372991MaxidolBAYER INCTCD-8478 · Presentationactive

Naproxen Sodium 220mg · ATC M01AE02 · AIG 0113934003

Structured fields (debug view: raw GS1 code → decoded)

FieldRaw valueDecodedNote
shortDescriptionEnglishMaxidol Liquid Gels 20svendor free text — not a structured field
shortDescriptionFrenchMaxidol Gélules Liquides 20vendor free text
size / sizeUOM20.0 EA20.0 unit(s)net content of the consumer unit — SNOMED pack size
packagingFormQualBOXBox or cartonmap to SNOMED unit of presentation / package type
packagingMaterialQual34Fibre (paperboard)
rxDosageFormTABSTabletsingle structured field — generic when alone
rxRouteOfAdministrationOROralseparate structured field — disambiguates the dose form for SNOMED (e.g. cutaneous vs vaginal cream)
status (derived)activediscontinued if any content version has a past discontinueDate; absence ≠ marketed — DPD gates the DIN
discontinueDate—
dateAvailable / dateEffective— / 2012-05-18first ship / first order
identification.dateUpdated2021-04-06T14:07:03.647-04:00
pharmaceuticalStatus / excellenceLevelCertified / 1Level 1 = brand-owner certified
dataProviderNameBayer Inc. Consumer Health
component dialect / versionsflat / 7flat dialect (single 114 node) carries no hierarchy
semantic_key02372991|20|EA|BOX|TABS|ORdin|size|uom|packForm|doseForm|route — duplicate detection key

The card wording “Tablet · Oral” is composed from the two separate structured fields above; descriptions like “Topical Cream” are vendor free text. For SNOMED, take the manufactured dose form from rxDosageForm and qualify it with rxRouteOfAdministration (compare Canesten DIN 02150867: CREA + TO topical, vs DIN 02150905: CREA + VA vaginal).

Packaging tree (1 component)

  • 114Dosageqty 1level 1 · seq 1 · 2 images

componentIdentification = level · sequence · type; indentation follows contextIdentification (parent). Types: Product = packaging/content level, Dosage = the dose-form units, Accessories = devices (applicator, dosing cup), Peel/Leaflet. This record uses the flat legacy dialect (single 114 node, no hierarchy).

Raw GS1 content (latest certified version, as ingested)
{
  "extendedDescriptionEnglish": "Maxidol Liquid Gels",
  "shortDescriptionEnglish": "Maxidol  Liquid Gels 20s",
  "productLabelType": "BR",
  "drugType": "T1",
  "controlledDrug": "CON4",
  "narcotic": "NAR4",
  "targetedSubstance": "No",
  "federalReportable": "No",
  "precursorStatus": "PN",
  "tempControlRangeMin": "20",
  "tempControlRangeMax": "25",
  "tempControlRangeUOM": "CE",
  "labelStorageConditionsEnglish": "Store between 20C and 25C",
  "labelStorageConditionsFrench": "Conserver entre 20C et 25C",
  "sterile": "No",
  "shakable": "Yes",
  "colourDescriptionEnglish": "Teal",
  "colourDescriptionFrench": "Sarcelle",
  "flavourDescriptionEnglish": "n/a",
  "flavourDescriptionFrench": "n/a",
  "dateEffective": "2012-05-18",
  "totalUnits": "1",
  "length": "4.32",
  "lengthUOM": "CM",
  "width": "9.27",
  "widthUOM": "CM",
  "height": "4.32",
  "heightUOM": "CM",
  "volume": "173.0",
  "volumeUOM": "CC",
  "grossWeight": "0.054",
  "grossWeightUOM": "K",
  "packagingFormQual": "BOX",
  "packagingMaterialQual": "34",
  "size": "20.0",
  "sizeUOM": "EA",
  "originOfProductCountry": "US",
  "gpcClassificationCode": "10000856",
  "barcodeSymbology": "34",
  "productType": "EA",
  "hazardRatingSystemWHMISclassCode": [],
  "rxDosageForm": "TABS",
  "rxRouteOfAdministration": "OR",
  "anatomicalTherapeuticChemical": "M01AE02",
  "markingLotNumber": "Y",
  "drugMerchandising": "UN",
  "drugMerchandisingBC": "UN",
  "drugMerchandisingMB": "UN",
  "drugMerchandisingNB": "UN",
  "drugMerchandisingNF": "UN",
  "drugMerchandisingNS": "UN",
  "drugMerchandisingNT": "UN",
  "drugMerchandisingNU": "UN",
  "drugMerchandisingON": "UN",
  "drugMerchandisingPEI": "UN",
  "drugMerchandisingPQ": "BC",
  "drugMerchandisingSK": "UN",
  "drugMerchandisingYK": "UN",
  "shortDescriptionFrench": "Maxidol  Gélules Liquides 20",
  "extendedDescriptionFrench": "Maxidol Gélules Liquides",
  "brand": "Maxidol",
  "brandFrench": "Maxidol",
  "markingExpiryDate": "Yes",
  "drugAndHealthProductGroup": [
    {
      "ahfs": [
        "28:08.04.92"
      ],
      "drugAndHealthProductNumber": "02372991",
      "aiGroupNumber": "0113934003",
      "drugAndHealthProductNumberType": "DIN",
      "activeIngredientGroup": [
        {
          "activeIngredientNameEnglish": "Naproxen Sodium",
          "activeIngredientStrength": "220",
          "activeIngredientStrengthUOM": "ME"
        }
      ]
    }
  ],
  "gpcClass": "Pain Relief Products",
  "gpcDescription": "General/Multi-use Pain Relief",
  "gpcFamily": "Health Treatments/Aids",
  "gpcSegment": "Healthcare",
  "pharmaceuticalComponent": [
    {
      "gtin1": "00056500363008",
      "componentQuantity": "1",
      "componentType": "4",
      "componentIdentification": "114",
      "contextIdentification": "0",
      "digitalAssetGroup": [
        {
          "digitalAssetFacingPharmaceutical": "1",
          "digitalAssetFormatPharmaceutical": "JPG",
          "digitalAssetGDTIPharmaceutical": "75400000002020000852055",
          "digitalAssetImageVersionDateTimePharmaceutical": "2018-07-17T18:52:45.000-04:00",
          "digitalAssetSequencePharmaceutical": "0"
        },
        {
          "digitalAssetFacingPharmaceutical": "7",
          "digitalAssetFormatPharmaceutical": "JPG",
          "digitalAssetGDTIPharmaceutical": "75400000002020000852141",
          "digitalAssetImageVersionDateTimePharmaceutical": "2018-07-17T18:52:45.000-04:00",
          "digitalAssetSequencePharmaceutical": "1"
        }
      ]
    }
  ],
  "identification": {
    "initialContentReceivedDate": "2018-07-17T18:52:45.000-04:00",
    "dateUpdated": "2021-04-06T14:07:03.647-04:00",
    "excellenceLevel": "1",
    "gln": "0056500000019",
    "gtin": "056500363008",
    "loadingOption": "7540000000999",
    "pharmaceuticalStatus": "Certified",
    "systemVersion": "2019-05-10T02:17:19.000-04:00"
  }
}