Eucalyptus 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
4964334705
5 mL in 1 VIAL, MULTI-DOSE (49643-347-05)
ndc11
4964334710
10 mL in 1 VIAL, MULTI-DOSE (49643-347-10)
ndc11
4964334730
30 mL in 1 VIAL, MULTI-DOSE (49643-347-30)
ndc11
4964334750
50 mL in 1 VIAL, MULTI-DOSE (49643-347-50)

Annotations

UNII (FDA Substance ID)

7XW7TB10X9

EUCALYPTUS GLOBULUS POLLEN

RxCUI 852386

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7XW7TB10X9",
    "rxcui": "852386",
    "inchikey": null,
    "display_name": "EUCALYPTUS GLOBULUS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "068ed8c0-1fff-42dd-a217-684201c16023": {
      "match": "brand_token",
      "title": "EUCALYPTUS SCENTED HAND SANITIZER (ALCOHOL) LIQUID [FOURSTAR GROUP USA, INC.]",
      "spl_version": "2",
      "published_date": "2025-02-27"
    }
  },
  "productid": "49643-347_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-347",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "EUCALYPTUS GLOBULUS POLLEN",
  "proprietary_name": "Eucalyptus Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Eucalyptus globulus",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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