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United States Β· US Β· US:22840-9411_36ac2d95-bfac-548b-e063-6394a90a749a
Elm Pollen Mix
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 3
- ndc11228409411210 mL in 1 VIAL, MULTI-DOSE (22840-9411-2)
- ndc11228409411450 mL in 1 VIAL, MULTI-DOSE (22840-9411-4)
- ndc1122840941155 mL in 1 BOTTLE, DROPPER (22840-9411-5)
Annotations
UNII (FDA Substance ID)
89BAT511BD
ULMUS AMERICANA POLLEN
RxCUI 852054
Raw payload (JSON)
{
"unii": {
"unii": "89BAT511BD",
"rxcui": "852054",
"inchikey": null,
"display_name": "ULMUS AMERICANA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-9411_36ac2d95-bfac-548b-e063-6394a90a749a",
"productndc": "22840-9411",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "ULMUS AMERICANA POLLEN; ULMUS PUMILA POLLEN",
"proprietary_name": "Elm Pollen Mix",
"active_ingred_unit": "g/mL; g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Ulmus americana and Ulmus pumila",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025; .025"
}Access this data programmatically
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