Universal WITCH HAZEL

UNIISPL

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

Identification

ManufacturerUniversal Distribution Center LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5200041406
177 mL in 1 BOTTLE, PLASTIC (52000-414-06)

Annotations

UNII (FDA Substance ID)

101I4J0U34

WITCH HAZEL

RxCUI 89821

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "101I4J0U34",
    "rxcui": "89821",
    "inchikey": null,
    "display_name": "WITCH HAZEL",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "183efdc2-cf3e-4f06-b292-0cfd097418b3": {
      "match": "brand_token",
      "title": "UNIVERSAL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]",
      "spl_version": "5",
      "published_date": "2026-02-27"
    }
  },
  "productid": "52000-414_66486f72-a425-450d-9669-0fa18a4899ee",
  "productndc": "52000-414",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "Universal WITCH HAZEL",
  "active_ingred_unit": "g/100mL",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "witch hazel",
  "start_marketing_date": "20230701",
  "active_numerator_strength": "3"
}

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