MIMIBO PREMIUM TOOTH

UNIISPL

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

Identification

ManufacturerCONE MEDICAL Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7352700041
20 g in 1 TUBE (73527-0004-1)

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": "DENTAL",
  "spl_meta": {
    "c101881a-5a12-2e04-e053-2a95a90a3f57": {
      "match": "brand_token",
      "title": "MIMIBO PREMIUM TOOTH (SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [CONE MEDICAL CO., LTD.]",
      "spl_version": "4",
      "published_date": "2025-01-06"
    }
  },
  "productid": "73527-0004_2ac515e8-9acc-e60f-e063-6394a90af897",
  "productndc": "73527-0004",
  "dosage_form": "PASTE, DENTIFRICE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": ".ALPHA.-TOCOPHEROL ACETATE; SILICON DIOXIDE; SODIUM PYROPHOSPHATE",
  "proprietary_name": "MIMIBO PREMIUM TOOTH",
  "active_ingred_unit": "g/100g; g/100g; g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Silicon Dioxide, Tocopherol Acetate, Tetrasodium Pyrophosphate",
  "start_marketing_date": "20210401",
  "active_numerator_strength": ".1; 14; .5"
}

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