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United States · US · US:59883-720_0a95fcbe-e811-031d-e063-6294a90aec1b

Pro-Den Rx

UNIISPLATC A01AA04

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerDen-mat Holdings, Llc
CountryUS (United States)
ATC codeA01AA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5988372008
    1 BOTTLE in 1 CARTON (59883-720-08) / 283.5 g in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
3FTR44B32Q
STANNOUS FLUORIDE
RxCUI 10030
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "3FTR44B32Q",
    "rxcui": "10030",
    "inchikey": "ANOBYBYXJXCGBS-UHFFFAOYSA-L",
    "display_name": "STANNOUS FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9036aa8a-59b1-41b0-b3cb-529d3303a1c0": {
      "match": "brand_token",
      "title": "PRO-DEN RX (STANNOUS FLUORIDE) RINSE [DEN-MAT HOLDINGS, LLC]",
      "spl_version": "6",
      "published_date": "2023-12-18"
    }
  },
  "productid": "59883-720_0a95fcbe-e811-031d-e063-6294a90aec1b",
  "productndc": "59883-720",
  "dosage_form": "RINSE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STANNOUS FLUORIDE",
  "proprietary_name": "Pro-Den Rx",
  "active_ingred_unit": "mg/g",
  "application_number": "M021",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Stannous Fluoride",
  "start_marketing_date": "20081031",
  "active_numerator_strength": "1.53"
}

Related drugs

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