White Ash 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
4964335705
5 mL in 1 VIAL, MULTI-DOSE (49643-357-05)
ndc11
4964335710
10 mL in 1 VIAL, MULTI-DOSE (49643-357-10)
ndc11
4964335730
30 mL in 1 VIAL, MULTI-DOSE (49643-357-30)
ndc11
4964335750
50 mL in 1 VIAL, MULTI-DOSE (49643-357-50)

Annotations

UNII (FDA Substance ID)

G684LX721Q

FRAXINUS AMERICANA POLLEN

RxCUI 852450

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G684LX721Q",
    "rxcui": "852450",
    "inchikey": null,
    "display_name": "FRAXINUS AMERICANA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "6f8b77c3-9833-4c75-b41c-a2bc12616157": {
      "match": "brand_token",
      "title": "WHITE GLO PURPLE COLOR CORRECTOR FLUORIDE ANTICAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [WHITE GLO USA INC]",
      "spl_version": "1",
      "published_date": "2026-05-21"
    }
  },
  "productid": "49643-357_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-357",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "FRAXINUS AMERICANA POLLEN",
  "proprietary_name": "White Ash Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Fraxinus americana",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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