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United States Β· US Β· US:22840-9352_36ac4a35-6d7b-a249-e063-6294a90a0b70
Plantain Sorrel Mix
UNIISPL
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· 2
- ndc11228409352210 mL in 1 VIAL, MULTI-DOSE (22840-9352-2)
- ndc11228409352450 mL in 1 VIAL, MULTI-DOSE (22840-9352-4)
Annotations
UNII (FDA Substance ID)
DO87T1U2CI
PLANTAGO LANCEOLATA POLLEN
RxCUI 852742
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "DO87T1U2CI",
"rxcui": "852742",
"inchikey": null,
"display_name": "PLANTAGO LANCEOLATA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"26facd12-ab50-e2c4-e063-6394a90ae8d1": {
"match": "brand_token",
"title": "PLANTAIN BEESWAX OINTMENT [URIEL PHARMACY INC.]",
"spl_version": "2",
"published_date": "2025-01-09"
}
},
"productid": "22840-9352_36ac4a35-6d7b-a249-e063-6294a90a0b70",
"productndc": "22840-9352",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "PLANTAGO LANCEOLATA POLLEN; RUMEX ACETOSELLA POLLEN",
"proprietary_name": "Plantain Sorrel Mix",
"active_ingred_unit": "g/mL; g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Plantago lanceolata and Rumex acetosella",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025; .025"
}Access this data programmatically
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