Black 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
2284054482
10 mL in 1 VIAL, MULTI-DOSE (22840-5448-2)
ndc11
2284054484
50 mL in 1 VIAL, MULTI-DOSE (22840-5448-4)
ndc11
2284054485
5 mL in 1 BOTTLE, DROPPER (22840-5448-5)

Annotations

UNII (FDA Substance ID)

294L626TT0

QUERCUS VELUTINA POLLEN

RxCUI 852260

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "294L626TT0",
    "rxcui": "852260",
    "inchikey": null,
    "display_name": "QUERCUS VELUTINA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "52910220-75f6-23d5-e063-6394a90a9ff3": {
      "match": "brand_token",
      "title": "BLACK GIRL SUNSCREEN MAKE IT POP RED WINE (ZINC OXIDE) LOTION [BLACK GIRL SUNSCREEN]",
      "spl_version": "1",
      "published_date": "2026-05-26"
    }
  },
  "productid": "22840-5448_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-5448",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "QUERCUS VELUTINA POLLEN",
  "proprietary_name": "Black Oak Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Quercus velutina",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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