Witch Hazel

UNIISPL

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

Identification

ManufacturerMedical Products Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1073380108
236 mL in 1 BOTTLE, DISPENSING (10733-801-08)

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": {
    "c50d0496-6f09-43c2-9383-3250885968c9": {
      "match": "brand_token",
      "title": "WITCH HAZEL LIQUID [AMERICAN SALES COMPANY]",
      "spl_version": "16",
      "published_date": "2026-05-01"
    }
  },
  "productid": "10733-801_28dabfcb-f8d9-6b91-e063-6394a90a800c",
  "productndc": "10733-801",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "Witch Hazel",
  "active_ingred_unit": "g/100mL",
  "application_number": "M015",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Witch Hazel",
  "start_marketing_date": "20210129",
  "active_numerator_strength": "86"
}

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