White Poplar 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
4964339405
5 mL in 1 VIAL, MULTI-DOSE (49643-394-05)
ndc11
4964339410
10 mL in 1 VIAL, MULTI-DOSE (49643-394-10)
ndc11
4964339430
30 mL in 1 VIAL, MULTI-DOSE (49643-394-30)
ndc11
4964339450
50 mL in 1 VIAL, MULTI-DOSE (49643-394-50)

Annotations

UNII (FDA Substance ID)

VU8C8SB23P

POPULUS ALBA POLLEN

RxCUI 852382

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "VU8C8SB23P",
    "rxcui": "852382",
    "inchikey": null,
    "display_name": "POPULUS ALBA 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": "49643-394_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-394",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "POPULUS ALBA POLLEN",
  "proprietary_name": "White Poplar Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Populus alba",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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