DENTI BUONGIORNO GUM CARE TOOTH

UNIISPL

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

Identification

ManufacturerDONG IL PHARMS CO.,LTD

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7324211182
1 TUBE in 1 CARTON (73242-1118-2) / 100 g in 1 TUBE (73242-1118-1)

Annotations

UNII (FDA Substance ID)

9E8X80D2L0

.ALPHA.-TOCOPHEROL ACETATE

RxCUI 1046243

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9E8X80D2L0",
    "rxcui": "1046243",
    "inchikey": null,
    "display_name": ".ALPHA.-TOCOPHEROL ACETATE",
    "substance_type": "mixture",
    "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": "73242-1118_4115f17d-6a1d-1db4-e063-6294a90a4a5d",
  "productndc": "73242-1118",
  "dosage_form": "PASTE, DENTIFRICE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": ".ALPHA.-TOCOPHEROL ACETATE; SILICON DIOXIDE; SODIUM FLUORIDE",
  "proprietary_name": "DENTI BUONGIORNO GUM CARE TOOTH",
  "active_ingred_unit": "g/100g; g/100g; g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Silica, Sodium Fluoride, Tocopheryl Acetate",
  "start_marketing_date": "20250401",
  "active_numerator_strength": ".2; 15; .22"
}

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