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United States · US · US:22840-5744_36abfd47-fc5e-43c4-e063-6394a90a8731
White Potato
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
- ndc11228405744210 mL in 1 VIAL, MULTI-DOSE (22840-5744-2)
- ndc1122840574455 mL in 1 BOTTLE, DROPPER (22840-5744-5)
Annotations
UNII (FDA Substance ID)
CFE1S8DYWD
POTATO
RxCUI 892632
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "CFE1S8DYWD",
"rxcui": "892632",
"inchikey": null,
"display_name": "POTATO",
"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": "22840-5744_36abfd47-fc5e-43c4-e063-6394a90a8731",
"productndc": "22840-5744",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "POTATO",
"proprietary_name": "White Potato",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Solanum tuberosum",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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