DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH

UNIISPLATC A01AA

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

Identification

ManufacturerDONG IL PHARMS CO.,LTD

CountryUS (United States)

ATC codeA01AA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7324211282
1 TUBE in 1 CARTON (73242-1128-2) / 100 g in 1 TUBE (73242-1128-1)

Annotations

UNII (FDA Substance ID)

ETJ7Z6XBU4

SILICON DIOXIDE

RxCUI 9771

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "ETJ7Z6XBU4",
    "rxcui": "9771",
    "inchikey": "VYPSYNLAJGMNEJ-UHFFFAOYSA-N",
    "display_name": "SILICON DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "487cd5b9-28f3-392d-e063-6394a90a9ba1": {
      "match": "brand_token",
      "title": "DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH (SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [DONG IL PHARMS CO.,LTD]",
      "spl_version": "1",
      "published_date": "2026-01-19"
    }
  },
  "productid": "73242-1128_487d9d48-6b2c-8a64-e063-6294a90a732e",
  "productndc": "73242-1128",
  "dosage_form": "PASTE, DENTIFRICE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE",
  "proprietary_name": "DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Silica, Sodium Monofluorophosphate",
  "start_marketing_date": "20260102",
  "active_numerator_strength": "18; .76"
}

Related drugs

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