medicated pads

UNIISPL

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

Identification

ManufacturerTARGET CORPORATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1167361410
100 PATCH in 1 BOX (11673-614-10) / 50 mg in 1 PATCH

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": {
    "52d0b36c-b65e-00cf-e063-6294a90ad089": {
      "match": "brand_token",
      "title": "MEDICATED CALLUS REMOVERS (SALICYLIC ACID) PATCH [PREMIER BRANDS OF AMERICA INC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "11673-614_412203ce-d7fc-28ee-e063-6394a90a929f",
  "productndc": "11673-614",
  "dosage_form": "PATCH",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "medicated pads",
  "active_ingred_unit": "mg/100mg",
  "application_number": "M015",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Witch Hazel",
  "start_marketing_date": "20200515",
  "active_numerator_strength": "50"
}

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