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United States · US · US:22840-1495_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
- ndc11228401495210 mL in 1 VIAL, MULTI-DOSE (22840-1495-2)
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": "22840-1495_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-1495",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "ULMUS CRASSIFOLIA POLLEN",
"proprietary_name": "Cedar Elm Pollen",
"active_ingred_unit": "[PNU]/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Ulmus crassifolia",
"start_marketing_date": "19810915",
"active_numerator_strength": "20000"
}Access this data programmatically
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