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United States · US · US:22840-2475_36ac4a35-6d79-a249-e063-6294a90a0b70
White Mulberry 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 · 2
- ndc11228402475210 mL in 1 VIAL, MULTI-DOSE (22840-2475-2)
- ndc11228402475450 mL in 1 VIAL, MULTI-DOSE (22840-2475-4)
Annotations
UNII (FDA Substance ID)
3I9T68187H
MORUS ALBA POLLEN
RxCUI 852669
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3I9T68187H",
"rxcui": "852669",
"inchikey": null,
"display_name": "MORUS 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": "22840-2475_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-2475",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "MORUS ALBA POLLEN",
"proprietary_name": "White Mulberry Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Morus alba",
"start_marketing_date": "19810915",
"active_numerator_strength": ".1"
}Access this data programmatically
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