Enamelon

UNIISPLATC A01AA04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerPremier Dental Products Company

CountryUS (United States)

ATC codeA01AA04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4878352043
1 TUBE in 1 CARTON (48783-520-43) / 122 g in 1 TUBE

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": "DENTAL",
  "spl_meta": {
    "04c3f178-7905-404d-9ac2-67c453287ddf": {
      "match": "brand_token",
      "title": "ENAMELON PREVENTIVE TREATMENT (STANNOUS FLUORIDE) GEL [PREMIER DENTAL PRODUCTS COMPANY]",
      "spl_version": "8",
      "published_date": "2026-01-14"
    }
  },
  "productid": "48783-520_4847e71b-2083-917b-e063-6394a90a2df0",
  "productndc": "48783-520",
  "dosage_form": "PASTE, DENTIFRICE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STANNOUS FLUORIDE",
  "proprietary_name": "Enamelon",
  "active_ingred_unit": "g/g",
  "application_number": "M021",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "stannous fluoride",
  "start_marketing_date": "20140101",
  "active_numerator_strength": ".00454"
}

Related drugs

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