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United States · US · US:22840-3408_36ac4a35-6d79-a249-e063-6294a90a0b70

White Oak 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 · 2

  • ndc11
    2284034082
    10 mL in 1 VIAL, MULTI-DOSE (22840-3408-2)
  • ndc11
    2284034084
    50 mL in 1 VIAL, MULTI-DOSE (22840-3408-4)

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": "22840-3408_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-3408",
  "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": ".1"
}

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