American Beech Pollen

UNIISPL

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

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
2284044342
10 mL in 1 VIAL, MULTI-DOSE (22840-4434-2)

Annotations

UNII (FDA Substance ID)

34X886W1H4

FAGUS GRANDIFOLIA POLLEN

RxCUI 852419

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "34X886W1H4",
    "rxcui": "852419",
    "inchikey": null,
    "display_name": "FAGUS GRANDIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "29299c46-a929-0d92-e063-6294a90a4218": {
      "match": "brand_token",
      "title": "AMERICAN RED CROSS 6OZ, 3% HYDROGEN PEROXIDE (AMERICAN RED CROSS 6 OZ, 3% HYDROGEN PEROXIDE SPRAY) SPRAY [MY IMPORTS USA LLC]",
      "spl_version": "3",
      "published_date": "2026-03-04"
    }
  },
  "productid": "22840-4434_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-4434",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "FAGUS GRANDIFOLIA POLLEN",
  "proprietary_name": "American Beech Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Fagus grandifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".1"
}

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