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United States Β· US Β· US:22840-1473_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 codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 2

  • ndc11
    2284014732
    10 mL in 1 VIAL, MULTI-DOSE (22840-1473-2)
  • ndc11
    2284014734
    50 mL in 1 VIAL, MULTI-DOSE (22840-1473-4)

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": "22840-1473_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-1473",
  "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": ".05"
}

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Salt Cedar Tamarisk Pollen (US) β€” Drug Database