Alpha-Pro

UNIISPL

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

Identification

ManufacturerDental Technologies, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5534609421
497 g in 1 BOTTLE (55346-0942-1)

Annotations

UNII (FDA Substance ID)

RGL5YE86CZ

HYDROFLUORIC ACID

RxCUI 5496

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "RGL5YE86CZ",
    "rxcui": "5496",
    "inchikey": "KRHYYFGTRYWZRS-UHFFFAOYSA-N",
    "display_name": "HYDROFLUORIC ACID",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "DENTAL",
  "spl_meta": {
    "a86ec65f-f6e1-474d-aeff-412a4716a92c": {
      "match": "brand_token",
      "title": "ALPHA-PRO (SODIUM FLUORIDE AND HYDROFLUORIC ACID) GEL [DENTAL TECHNOLOGIES, INC.]",
      "spl_version": "3",
      "published_date": "2025-11-17"
    }
  },
  "productid": "55346-0942_42c8ae03-7559-51a8-e063-6394a90ab69e",
  "productndc": "55346-0942",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYDROFLUORIC ACID; SODIUM FLUORIDE",
  "proprietary_name": "Alpha-Pro",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Sodium Fluoride and Hydrofluoric Acid",
  "start_marketing_date": "20130401",
  "active_numerator_strength": "4.4; 7.9"
}

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