White Birch 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 · 2

ndc11
2284014582
10 mL in 1 VIAL, MULTI-DOSE (22840-1458-2)
ndc11
2284014584
50 mL in 1 VIAL, MULTI-DOSE (22840-1458-4)

Annotations

UNII (FDA Substance ID)

23H70FYJ5U

BETULA POPULIFOLIA POLLEN

RxCUI 852178

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "23H70FYJ5U",
    "rxcui": "852178",
    "inchikey": null,
    "display_name": "BETULA POPULIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "6f8b77c3-9833-4c75-b41c-a2bc12616157": {
      "match": "brand_token",
      "title": "WHITE GLO PURPLE COLOR CORRECTOR FLUORIDE ANTICAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [WHITE GLO USA INC]",
      "spl_version": "1",
      "published_date": "2026-05-21"
    }
  },
  "productid": "22840-1458_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-1458",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA POPULIFOLIA POLLEN",
  "proprietary_name": "White Birch Pollen",
  "active_ingred_unit": "[PNU]/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Betula populifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": "20000"
}

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