White Oak 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 · 3

ndc11
2284054822
10 mL in 1 VIAL, MULTI-DOSE (22840-5482-2)
ndc11
2284054824
50 mL in 1 VIAL, MULTI-DOSE (22840-5482-4)
ndc11
2284054825
5 mL in 1 BOTTLE, DROPPER (22840-5482-5)

Annotations

UNII (FDA Substance ID)

Z4Y9ZSV4KK

QUERCUS ALBA POLLEN

RxCUI 852294

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Z4Y9ZSV4KK",
    "rxcui": "852294",
    "inchikey": null,
    "display_name": "QUERCUS ALBA 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": "22840-5482_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-5482",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "QUERCUS ALBA POLLEN",
  "proprietary_name": "White Oak Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Quercus alba",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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