DOCTRUST K Tooth

UNIISPLATC A01AA

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

Identification

ManufacturerDOCSMEDI Co., Ltd.

CountryUS (United States)

ATC codeA01AA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7667000142
1 TUBE in 1 CARTON (76670-0014-2) / 60 g in 1 TUBE (76670-0014-1)

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": "DENTAL",
  "spl_meta": {
    "4476923a-48f1-9f72-e063-6394a90a0708": {
      "match": "brand_token",
      "title": "DOCTRUST ONE S TOOTH (SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE) PASTE, DENTIFRICE [DONG IL PHARMS CO.,LTD]",
      "spl_version": "1",
      "published_date": "2025-11-26"
    }
  },
  "productid": "76670-0014_2c484532-89d7-c8d3-e063-6294a90a793d",
  "productndc": "76670-0014",
  "dosage_form": "GEL, DENTIFRICE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE",
  "proprietary_name": "DOCTRUST K Tooth",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Silicon dioxide, Sodium monofluorophosphate",
  "start_marketing_date": "20221201",
  "active_numerator_strength": "16; .74"
}

Related drugs

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