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United States · US · US:22840-5450_36ac4a35-6d79-a249-e063-6294a90a0b70
California Live Oak 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 · 3
- ndc11228405450210 mL in 1 VIAL, MULTI-DOSE (22840-5450-2)
- ndc11228405450450 mL in 1 VIAL, MULTI-DOSE (22840-5450-4)
- ndc1122840545055 mL in 1 BOTTLE, DROPPER (22840-5450-5)
Annotations
UNII (FDA Substance ID)
VOT5MA71M7
QUERCUS AGRIFOLIA POLLEN
RxCUI 852302
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "VOT5MA71M7",
"rxcui": "852302",
"inchikey": null,
"display_name": "QUERCUS AGRIFOLIA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"aa10dbbf-97b3-4258-bbd3-0d8cc9935e12": {
"match": "brand_token",
"title": "CALIFORNIA ALOE FRESH POW DERY SUN (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) STICK [NATURE REPUBLIC CO., LTD.]",
"spl_version": "5",
"published_date": "2026-01-14"
}
},
"productid": "22840-5450_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5450",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "QUERCUS AGRIFOLIA POLLEN",
"proprietary_name": "California Live Oak Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Quercus agrifolia",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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