Black Oak Pollen

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964345105
5 mL in 1 VIAL, MULTI-DOSE (49643-451-05)
ndc11
4964345110
10 mL in 1 VIAL, MULTI-DOSE (49643-451-10)
ndc11
4964345130
30 mL in 1 VIAL, MULTI-DOSE (49643-451-30)
ndc11
4964345150
50 mL in 1 VIAL, MULTI-DOSE (49643-451-50)

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": "CUTANEOUS; INTRADERMAL; 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": "49643-451_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-451",
  "dosage_form": "INJECTION",
  "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": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Quercus velutina",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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