Cauliflower

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
2284057132
10 mL in 1 VIAL, MULTI-DOSE (22840-5713-2)
ndc11
2284057135
5 mL in 1 BOTTLE, DROPPER (22840-5713-5)

Annotations

UNII (FDA Substance ID)

138LUT2DWV

CAULIFLOWER

RxCUI 899661

Raw payload (JSON)

{
  "unii": {
    "unii": "138LUT2DWV",
    "rxcui": "899661",
    "inchikey": null,
    "display_name": "CAULIFLOWER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-5713_36abfd47-fc5e-43c4-e063-6394a90a8731",
  "productndc": "22840-5713",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "CAULIFLOWER",
  "proprietary_name": "Cauliflower",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Brassica oleracea var. botrytis",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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