Spring Birch 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
4964344105
5 mL in 1 VIAL, MULTI-DOSE (49643-441-05)
ndc11
4964344110
10 mL in 1 VIAL, MULTI-DOSE (49643-441-10)
ndc11
4964344130
30 mL in 1 VIAL, MULTI-DOSE (49643-441-30)
ndc11
4964344150
50 mL in 1 VIAL, MULTI-DOSE (49643-441-50)

Annotations

UNII (FDA Substance ID)

R889N2L976

BETULA OCCIDENTALIS POLLEN

RxCUI 852166

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "R889N2L976",
    "rxcui": "852166",
    "inchikey": null,
    "display_name": "BETULA OCCIDENTALIS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "294051e3-69ec-4190-8b03-fa34988376b7": {
      "match": "brand_token",
      "title": "SPRING GENE OIL PULLING SENSITIVITY (POTASSIUM NITRATE) PASTE, DENTIFRICE [HEALTH AND NATURAL BEAUTY USA CORP]",
      "spl_version": "1",
      "published_date": "2026-03-30"
    }
  },
  "productid": "49643-441_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-441",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA OCCIDENTALIS POLLEN",
  "proprietary_name": "Spring Birch Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Betula fontinalis",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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