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United States · US · US:22840-9306_36ac4a35-6d7b-a249-e063-6294a90a0b70
3 Weed Mix
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11228409306210 mL in 1 VIAL, MULTI-DOSE (22840-9306-2)
- ndc11228409306450 mL in 1 VIAL, MULTI-DOSE (22840-9306-4)
- ndc1122840930655 mL in 1 BOTTLE, DROPPER (22840-9306-5)
Annotations
UNII (FDA Substance ID)
73B14PX5FW
AMARANTHUS RETROFLEXUS POLLEN
RxCUI 851930
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "73B14PX5FW",
"rxcui": "851930",
"inchikey": null,
"display_name": "AMARANTHUS RETROFLEXUS POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"ddc59e50-083a-6cd9-e053-2995a90ad401": {
"match": "brand_token",
"title": "3 HYDROGEN PEROXIDE (HYDROGEN PEROXIDE) LIQUID [JELL PHARMACEUTICALS PVT LTD.]",
"spl_version": "5",
"published_date": "2025-09-29"
}
},
"productid": "22840-9306_36ac4a35-6d7b-a249-e063-6294a90a0b70",
"productndc": "22840-9306",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AMARANTHUS RETROFLEXUS POLLEN; CHENOPODIUM ALBUM POLLEN; XANTHIUM STRUMARIUM POLLEN",
"proprietary_name": "3 Weed Mix",
"active_ingred_unit": "g/mL; g/mL; g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Xanthium strumarium, Chenopodium album, Amaranthus retroflexus",
"start_marketing_date": "19810915",
"active_numerator_strength": ".01666; .01666; .01666"
}Access this data programmatically
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