Gray (White) 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
4964332505
5 mL in 1 VIAL, MULTI-DOSE (49643-325-05)
ndc11
4964332510
10 mL in 1 VIAL, MULTI-DOSE (49643-325-10)
ndc11
4964332530
30 mL in 1 VIAL, MULTI-DOSE (49643-325-30)
ndc11
4964332550
50 mL in 1 VIAL, MULTI-DOSE (49643-325-50)

Annotations

UNII (FDA Substance ID)

23H70FYJ5U

BETULA POPULIFOLIA POLLEN

RxCUI 852178

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "23H70FYJ5U",
    "rxcui": "852178",
    "inchikey": null,
    "display_name": "BETULA POPULIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "3c41ed29-d5e6-fefb-e063-6294a90a2d11": {
      "match": "brand_token",
      "title": "GRAY NAIL ESSENCE OIL (PEPPERMINT OIL 1%) LIQUID [GUANGZHOU CHUANMA INTERNATIONAL TRADING CO.,LTD.]",
      "spl_version": "1",
      "published_date": "2025-08-15"
    }
  },
  "productid": "49643-325_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-325",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA POPULIFOLIA POLLEN",
  "proprietary_name": "Gray (White) Birch Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Betula populifolia",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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