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United States · US · US:22840-1471_36ac4a35-6d79-a249-e063-6294a90a0b70
Salt Cedar Tamarisk Pollen
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 · 2
- ndc11228401471210 mL in 1 VIAL, MULTI-DOSE (22840-1471-2)
- ndc11228401471450 mL in 1 VIAL, MULTI-DOSE (22840-1471-4)
Annotations
UNII (FDA Substance ID)
43IR7KR479
TAMARIX GALLICA POLLEN
RxCUI 852083
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "43IR7KR479",
"rxcui": "852083",
"inchikey": null,
"display_name": "TAMARIX GALLICA POLLEN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"spl_meta": {
"4fae649d-f60e-0275-e063-6294a90a1ea5": {
"match": "brand_token",
"title": "SALT WATER VANILLA SUNSCREEN BODY BROAD SPECTRUM SPF 50 (SUNSCREEN) OIL [SALTAIR BODY LLC]",
"spl_version": "1",
"published_date": "2026-04-20"
}
},
"productid": "22840-1471_36ac4a35-6d79-a249-e063-6294a90a0b70",
"productndc": "22840-1471",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "TAMARIX GALLICA POLLEN",
"proprietary_name": "Salt Cedar Tamarisk Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Tamarix gallica",
"start_marketing_date": "19810915",
"active_numerator_strength": ".1"
}Access this data programmatically
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