Sunflower

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
2284015032
10 mL in 1 VIAL, MULTI-DOSE (22840-1503-2)
ndc11
2284015034
50 mL in 1 VIAL, MULTI-DOSE (22840-1503-4)

Annotations

UNII (FDA Substance ID)

28D6K7E9IP

HELIANTHUS ANNUUS POLLEN

RxCUI 852509

Raw payload (JSON)

{
  "unii": {
    "unii": "28D6K7E9IP",
    "rxcui": "852509",
    "inchikey": null,
    "display_name": "HELIANTHUS ANNUUS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-1503_36abfd47-fc5d-43c4-e063-6394a90a8731",
  "productndc": "22840-1503",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "HELIANTHUS ANNUUS POLLEN",
  "proprietary_name": "Sunflower",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Helianthus annuus",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".1"
}

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