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United States · US · US:22840-1496_36ac4a35-6d79-a249-e063-6294a90a0b70

Cedar Elm 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 · 1

  • ndc11
    2284014961
    5 mL in 1 VIAL, MULTI-DOSE (22840-1496-1)

Annotations

UNII (FDA Substance ID)
G82398SD3I
ULMUS CRASSIFOLIA POLLEN
RxCUI 1014191
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "G82398SD3I",
    "rxcui": "1014191",
    "inchikey": null,
    "display_name": "ULMUS CRASSIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "8ab87e13-99ad-4b25-a0c3-e46a868cc684": {
      "match": "brand_token",
      "title": "CEDAR X FORMULA (OLIBANUM, THUJA OCCIDENTALIS, GELSEMIUM SEMPERVIRENS, ALLIUM CEPA, ANTIMONIUM TARTARICUM, HEPAR SULPHURIS CALCAREUM, JUNIPERUS COMMUNIS.) LIQUID [INTEGRATIVE HEALING INSTITUTE, LLC]",
      "spl_version": "6",
      "published_date": "2025-11-17"
    }
  },
  "productid": "22840-1496_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-1496",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "ULMUS CRASSIFOLIA POLLEN",
  "proprietary_name": "Cedar Elm Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Ulmus crassifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".001"
}

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