White Mulbery 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
4964338205
5 mL in 1 VIAL, MULTI-DOSE (49643-382-05)
ndc11
4964338210
10 mL in 1 VIAL, MULTI-DOSE (49643-382-10)
ndc11
4964338230
30 mL in 1 VIAL, MULTI-DOSE (49643-382-30)
ndc11
4964338250
50 mL in 1 VIAL, MULTI-DOSE (49643-382-50)

Annotations

UNII (FDA Substance ID)

3I9T68187H

MORUS ALBA POLLEN

RxCUI 852669

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3I9T68187H",
    "rxcui": "852669",
    "inchikey": null,
    "display_name": "MORUS 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": "49643-382_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-382",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "MORUS ALBA POLLEN",
  "proprietary_name": "White Mulbery Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Morus alba",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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