Hazel Alder Pollen

UNIISPL

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

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
2284054021
5 mL in 1 VIAL, MULTI-DOSE (22840-5402-1)
ndc11
2284054022
10 mL in 1 VIAL, MULTI-DOSE (22840-5402-2)
ndc11
2284054024
50 mL in 1 VIAL, MULTI-DOSE (22840-5402-4)

Annotations

UNII (FDA Substance ID)

390VZ1D0L5

ALNUS SERRULATA POLLEN

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "390VZ1D0L5",
    "rxcui": null,
    "inchikey": null,
    "display_name": "ALNUS SERRULATA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "314b75cb-affe-a248-e063-6294a90a47b7": {
      "match": "brand_token",
      "title": "HAZEL PERINEAL HEALING FOAM (WITCH HAZEL) LIQUID [JIANGSU SENWO MEDICAL TECHNOLOGY CO., LTD.]",
      "spl_version": "4",
      "published_date": "2026-01-16"
    }
  },
  "productid": "22840-5402_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-5402",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "ALNUS SERRULATA POLLEN",
  "proprietary_name": "Hazel Alder Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Alnus serrulata",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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