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United States · US · US:22840-1462_36ac4a35-6d79-a249-e063-6294a90a0b70
White Birch 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
- ndc1122840146215 mL in 1 VIAL, MULTI-DOSE (22840-1462-1)
Annotations
UNII (FDA Substance ID)
23H70FYJ5U
BETULA POPULIFOLIA POLLEN
RxCUI 852178
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "23H70FYJ5U",
"rxcui": "852178",
"inchikey": null,
"display_name": "BETULA POPULIFOLIA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"6f8b77c3-9833-4c75-b41c-a2bc12616157": {
"match": "brand_token",
"title": "WHITE GLO PURPLE COLOR CORRECTOR FLUORIDE ANTICAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [WHITE GLO USA INC]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "22840-1462_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-1462",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "BETULA POPULIFOLIA POLLEN",
"proprietary_name": "White Birch Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Betula populifolia",
"start_marketing_date": "19810915",
"active_numerator_strength": ".001"
}Access this data programmatically
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