TN Dickinsons Witch Hazel Astringent

UNIISPL

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

Identification

ManufacturerDickinson Brands Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
5265100104
3785 mL in 1 BOTTLE (52651-001-04)
ndc11
5265100105
237 mL in 1 BOTTLE, DISPENSING (52651-001-05)
ndc11
5265100106
473 mL in 1 BOTTLE, DISPENSING (52651-001-06)
ndc11
5265100107
59 mL in 1 BOTTLE (52651-001-07)

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": {
    "537c9c27-ee81-4920-8e3f-21edb844c9cf": {
      "match": "brand_token",
      "title": "TN DICKINSONS PAIN AND ITCH RELIEF (PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE) LIQUID [DICKINSON BRANDS INC.]",
      "spl_version": "2",
      "published_date": "2026-02-06"
    }
  },
  "productid": "52651-001_cee176f9-9862-4293-b5e7-5e93d201914c",
  "productndc": "52651-001",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "TN Dickinsons Witch Hazel Astringent",
  "active_ingred_unit": "g/100mL",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Witch Hazel",
  "start_marketing_date": "19891202",
  "active_numerator_strength": "86"
}

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