Black Willow 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
4964340905
5 mL in 1 VIAL, MULTI-DOSE (49643-409-05)
ndc11
4964340910
10 mL in 1 VIAL, MULTI-DOSE (49643-409-10)
ndc11
4964340930
30 mL in 1 VIAL, MULTI-DOSE (49643-409-30)
ndc11
4964340950
50 mL in 1 VIAL, MULTI-DOSE (49643-409-50)

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": "CUTANEOUS; INTRADERMAL; 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": "49643-409_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-409",
  "dosage_form": "INJECTION",
  "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": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Salix nigra",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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