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United States · US · US:49643-355_36ad1e17-751d-e226-e063-6394a90ab328
Desert Ragweed Pollen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1149643355055 mL in 1 VIAL, MULTI-DOSE (49643-355-05)
- ndc11496433551010 mL in 1 VIAL, MULTI-DOSE (49643-355-10)
- ndc11496433553030 mL in 1 VIAL, MULTI-DOSE (49643-355-30)
- ndc11496433555050 mL in 1 VIAL, MULTI-DOSE (49643-355-50)
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": "CUTANEOUS; INTRADERMAL; 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": "49643-355_36ad1e17-751d-e226-e063-6394a90ab328",
"productndc": "49643-355",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AMBROSIA DUMOSA POLLEN",
"proprietary_name": "Desert Ragweed Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA102211",
"marketing_category": "BLA",
"nonproprietary_name": "Ambrosia dumosa",
"start_marketing_date": "19740312",
"active_numerator_strength": ".05"
}Access this data programmatically
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