Nobaton 1.5%Fine Salt ampoule

UNIISPLATC A01AA

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

Identification

ManufacturerBD TECHNOLOGY CO.,LTD

CountryUS (United States)

ATC codeA01AA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7392700091
35 g in 1 TUBE (73927-0009-1)

Annotations

UNII (FDA Substance ID)

8NY9L8837D

OLAFLUR

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "8NY9L8837D",
    "rxcui": null,
    "inchikey": "ZVVSSOQAYNYNPP-UHFFFAOYSA-N",
    "display_name": "OLAFLUR",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "DENTAL",
  "spl_meta": {
    "3341ef2d-7fa5-b828-e063-6394a90ab191": {
      "match": "brand_token",
      "title": "NOBATON 1.5%FINE SALT AMPOULE (NOBATON 1.5%FINE SALT AMPOULE TOOTHPASTE) OINTMENT [BD TECHNOLOGY CO.,LTD]",
      "spl_version": "1",
      "published_date": "2025-04-23"
    }
  },
  "productid": "73927-0009_3341ef39-b2cf-a9a3-e063-6294a90ab223",
  "productndc": "73927-0009",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OLAFLUR; SODIUM MONOFLUOROPHOSPHATE",
  "proprietary_name": "Nobaton 1.5%Fine Salt ampoule",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Nobaton 1.5%Fine Salt ampoule toothpaste",
  "start_marketing_date": "20250421",
  "active_numerator_strength": ".0975; 1"
}

Related drugs

Other records sharing ATC code A01AA.

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