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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

  • ndc11
    2284057442
    10 mL in 1 VIAL, MULTI-DOSE (22840-5744-2)
  • ndc11
    2284057445
    5 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"
}

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