Salt Cedar Pollen

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964341505
5 mL in 1 VIAL, MULTI-DOSE (49643-415-05)
ndc11
4964341510
10 mL in 1 VIAL, MULTI-DOSE (49643-415-10)
ndc11
4964341530
30 mL in 1 VIAL, MULTI-DOSE (49643-415-30)
ndc11
4964341550
50 mL in 1 VIAL, MULTI-DOSE (49643-415-50)

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": "CUTANEOUS; INTRADERMAL; 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": "49643-415_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-415",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "TAMARIX GALLICA POLLEN",
  "proprietary_name": "Salt Cedar Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Tamarix gallica",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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