🇺🇸
United States · US · US:22840-3475_36ac4a35-6d79-a249-e063-6294a90a0b70
White Poplar 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
- ndc1122840347515 mL in 1 VIAL, MULTI-DOSE (22840-3475-1)
Annotations
UNII (FDA Substance ID)
VU8C8SB23P
POPULUS ALBA POLLEN
RxCUI 852382
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "VU8C8SB23P",
"rxcui": "852382",
"inchikey": null,
"display_name": "POPULUS ALBA 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": "22840-3475_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-3475",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "POPULUS ALBA POLLEN",
"proprietary_name": "White Poplar Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Populus alba",
"start_marketing_date": "19810915",
"active_numerator_strength": ".001"
}Access this data programmatically
Query White Poplar Pollen and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.