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United States · US · US:16571-814_82dc4f9f-0dc5-46f8-8deb-3966669470cd

Denta 5000 Plus

In shortageUNIISPLATC A01AA51

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeA01AA51
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1657181450
    51 g in 1 TUBE (16571-814-50)

Annotations

UNII (FDA Substance ID)
8ZYQ1474W7
SODIUM FLUORIDE
RxCUI 9873
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Sodium Oxybate Solution
Raw payload (JSON)
{
  "unii": {
    "unii": "8ZYQ1474W7",
    "rxcui": "9873",
    "inchikey": "PUZPDOWCWNUUKD-UHFFFAOYSA-M",
    "display_name": "SODIUM FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "585fb1f5-8c08-43bd-8be4-64adc065d9a2": {
      "match": "brand_token",
      "title": "DENTA 5000 PLUS SENSITIVE (SODIUM FLUORIDE AND POTASSIUM NITRATE) GEL, DENTIFRICE [RISING PHARMA HOLDINGS, INC.]",
      "spl_version": "1",
      "published_date": "2024-02-19"
    }
  },
  "productid": "16571-814_82dc4f9f-0dc5-46f8-8deb-3966669470cd",
  "productndc": "16571-814",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SODIUM FLUORIDE",
  "shortage_reason": "Sodium Oxybate Solution",
  "shortage_status": "current",
  "proprietary_name": "Denta 5000 Plus",
  "active_ingred_unit": "g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Sodium fluoride",
  "start_marketing_date": "20230703",
  "active_numerator_strength": "1.1"
}

Related drugs

Other records sharing ATC code A01AA51.

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