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United States Β· US Β· US:22840-1425_36ac4a35-6d79-a249-e063-6294a90a0b70

White Ash Pollen

UNIISPL

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

Identification

ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 2

  • ndc11
    2284014252
    10 mL in 1 VIAL, MULTI-DOSE (22840-1425-2)
  • ndc11
    2284014254
    50 mL in 1 VIAL, MULTI-DOSE (22840-1425-4)

Annotations

UNII (FDA Substance ID)
G684LX721Q
FRAXINUS AMERICANA POLLEN
RxCUI 852450
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "G684LX721Q",
    "rxcui": "852450",
    "inchikey": null,
    "display_name": "FRAXINUS AMERICANA 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": "22840-1425_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-1425",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "FRAXINUS AMERICANA POLLEN",
  "proprietary_name": "White Ash Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Fraxinus americana",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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White Ash Pollen (US) β€” Drug Database