California Juniper 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
4964336805
5 mL in 1 VIAL, MULTI-DOSE (49643-368-05)
ndc11
4964336810
10 mL in 1 VIAL, MULTI-DOSE (49643-368-10)
ndc11
4964336830
30 mL in 1 VIAL, MULTI-DOSE (49643-368-30)
ndc11
4964336850
50 mL in 1 VIAL, MULTI-DOSE (49643-368-50)

Annotations

UNII (FDA Substance ID)

0H1V4V5V9L

JUNIPERUS CALIFORNICA POLLEN

RxCUI 852585

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "0H1V4V5V9L",
    "rxcui": "852585",
    "inchikey": null,
    "display_name": "JUNIPERUS CALIFORNICA 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": "49643-368_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-368",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "JUNIPERUS CALIFORNICA POLLEN",
  "proprietary_name": "California Juniper Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Juniperus californica",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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