Black Willow Pollen

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
2284054782
10 mL in 1 VIAL, MULTI-DOSE (22840-5478-2)
ndc11
2284054784
50 mL in 1 VIAL, MULTI-DOSE (22840-5478-4)
ndc11
2284054785
5 mL in 1 BOTTLE, DROPPER (22840-5478-5)

Annotations

UNII (FDA Substance ID)

6M2JIH93ZN

SALIX NIGRA POLLEN

RxCUI 1014755

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6M2JIH93ZN",
    "rxcui": "1014755",
    "inchikey": null,
    "display_name": "SALIX NIGRA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "52910220-75f6-23d5-e063-6394a90a9ff3": {
      "match": "brand_token",
      "title": "BLACK GIRL SUNSCREEN MAKE IT POP RED WINE (ZINC OXIDE) LOTION [BLACK GIRL SUNSCREEN]",
      "spl_version": "1",
      "published_date": "2026-05-26"
    }
  },
  "productid": "22840-5478_36ac4a35-6d79-a249-e063-6294a90a0b70",
  "productndc": "22840-5478",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "SALIX NIGRA POLLEN",
  "proprietary_name": "Black Willow Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Salix nigra",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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