White Alder 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
2284044922
10 mL in 1 VIAL, MULTI-DOSE (22840-4492-2)
ndc11
2284044924
50 mL in 1 VIAL, MULTI-DOSE (22840-4492-4)

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": "22840-4492_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-4492",
  "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": ".1"
}

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