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United States · US · US:22840-1412_36ac4a35-6d79-a249-e063-6294a90a0b70

White Alder Pollen

UNIISPL

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

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
    2284014121
    5 mL in 1 VIAL, MULTI-DOSE (22840-1412-1)

Annotations

UNII (FDA Substance ID)
7X8HL8GRTM
ALNUS RHOMBIFOLIA POLLEN
RxCUI 851910
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7X8HL8GRTM",
    "rxcui": "851910",
    "inchikey": null,
    "display_name": "ALNUS RHOMBIFOLIA 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": "22840-1412_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-1412",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "ALNUS RHOMBIFOLIA POLLEN",
  "proprietary_name": "White Alder Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Alnus rhombifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".001"
}

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