Desert Ragweed

UNIISPL

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 · 1

ndc11
2284013771
5 mL in 1 VIAL, MULTI-DOSE (22840-1377-1)

Annotations

UNII (FDA Substance ID)

ZIO18VN6HJ

AMBROSIA DUMOSA POLLEN

RxCUI 851981

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "ZIO18VN6HJ",
    "rxcui": "851981",
    "inchikey": null,
    "display_name": "AMBROSIA DUMOSA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "ea36371a-b768-e335-e053-2a95a90a60a7": {
      "match": "brand_token",
      "title": "DESERT SUN PROTECTION BROAD SPECTRUM SPF30 (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [BOISE IMAGE ENHANCEMENT CENTRE PA]",
      "spl_version": "2",
      "published_date": "2024-01-17"
    }
  },
  "productid": "22840-1377_36ac4a35-6d7b-a249-e063-6294a90a0b70",
  "productndc": "22840-1377",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMBROSIA DUMOSA POLLEN",
  "proprietary_name": "Desert Ragweed",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Ambrosia dumosa",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".001"
}

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