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United States · US · US:22840-5451_36ac4a35-6d79-a249-e063-6294a90a0b70
California White 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
- ndc11228405451210 mL in 1 VIAL, MULTI-DOSE (22840-5451-2)
- ndc11228405451450 mL in 1 VIAL, MULTI-DOSE (22840-5451-4)
- ndc1122840545155 mL in 1 BOTTLE, DROPPER (22840-5451-5)
Annotations
UNII (FDA Substance ID)
HGH5K3653K
QUERCUS LOBATA POLLEN
RxCUI 1111024
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "HGH5K3653K",
"rxcui": "1111024",
"inchikey": null,
"display_name": "QUERCUS LOBATA 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": "22840-5451_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5451",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "QUERCUS LOBATA POLLEN",
"proprietary_name": "California White Oak Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Quercus lobata",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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