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United States Β· US Β· US:22840-5449_36ac4a35-6d79-a249-e063-6294a90a0b70
California Black Oak Pollen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 3
- ndc11228405449210 mL in 1 VIAL, MULTI-DOSE (22840-5449-2)
- ndc11228405449450 mL in 1 VIAL, MULTI-DOSE (22840-5449-4)
- ndc1122840544955 mL in 1 BOTTLE, DROPPER (22840-5449-5)
Annotations
UNII (FDA Substance ID)
02RVY6X9EC
QUERCUS KELLOGGII POLLEN
RxCUI 1014721
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "02RVY6X9EC",
"rxcui": "1014721",
"inchikey": null,
"display_name": "QUERCUS KELLOGGII 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": "22840-5449_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-5449",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "QUERCUS KELLOGGII POLLEN",
"proprietary_name": "California Black Oak Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Quercus kelloggii",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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