California Scrub Oak 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
4964340305
5 mL in 1 VIAL, MULTI-DOSE (49643-403-05)
ndc11
4964340310
10 mL in 1 VIAL, MULTI-DOSE (49643-403-10)
ndc11
4964340330
30 mL in 1 VIAL, MULTI-DOSE (49643-403-30)
ndc11
4964340350
50 mL in 1 VIAL, MULTI-DOSE (49643-403-50)

Annotations

UNII (FDA Substance ID)

P5W45RU6E4

QUERCUS DUMOSA POLLEN

RxCUI 852802

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "P5W45RU6E4",
    "rxcui": "852802",
    "inchikey": null,
    "display_name": "QUERCUS DUMOSA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "aa10dbbf-97b3-4258-bbd3-0d8cc9935e12": {
      "match": "brand_token",
      "title": "CALIFORNIA ALOE FRESH POW DERY SUN (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) STICK [NATURE REPUBLIC CO., LTD.]",
      "spl_version": "5",
      "published_date": "2026-01-14"
    }
  },
  "productid": "49643-403_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-403",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "QUERCUS DUMOSA POLLEN",
  "proprietary_name": "California Scrub Oak Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Quercus dumosa",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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