Birch Pollen Mix

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 · 2

ndc11
2284094032
10 mL in 1 VIAL, MULTI-DOSE (22840-9403-2)
ndc11
2284094034
50 mL in 1 VIAL, MULTI-DOSE (22840-9403-4)

Annotations

UNII (FDA Substance ID)

JQ5HI5004M

BETULA LENTA POLLEN

RxCUI 852144

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "JQ5HI5004M",
    "rxcui": "852144",
    "inchikey": null,
    "display_name": "BETULA LENTA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "0fa00042-b326-6d2d-e063-6394a90a236d": {
      "match": "brand_token",
      "title": "BIRCH JUNIPER LIQUID [URIEL PHARMACY INC]",
      "spl_version": "5",
      "published_date": "2025-11-19"
    }
  },
  "productid": "22840-9403_36ac2d95-bfac-548b-e063-6394a90a749a",
  "productndc": "22840-9403",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA LENTA POLLEN; BETULA NIGRA POLLEN; BETULA POPULIFOLIA POLLEN",
  "proprietary_name": "Birch Pollen Mix",
  "active_ingred_unit": "g/mL; g/mL; g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Betula lenta, Betula nigra and Betula populifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".0083333; .0083333; .0083333"
}

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