Humphreys Maravilla

UNIISPL

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

Identification

ManufacturerHumphreys Pharmacal, Incorporated

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0219020416
473 mL in 1 BOTTLE, PLASTIC (0219-0204-16)
ndc11
0219020480
237 mL in 1 BOTTLE, PLASTIC (0219-0204-80)

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": {
    "7d403bf4-8a0d-4337-8e81-1149cd0ae1dc": {
      "match": "brand_token",
      "title": "HUMPHREYS MARAVILLA (WITCH HAZEL) LIQUID [HUMPHREYS PHARMACAL, INCORPORATED]",
      "spl_version": "9",
      "published_date": "2024-12-12"
    }
  },
  "productid": "0219-0204_ceb593f8-3283-4375-a27e-50597a6468d8",
  "productndc": "0219-0204",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "Humphreys Maravilla",
  "active_ingred_unit": "g/mL",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "witch hazel",
  "start_marketing_date": "19550111",
  "active_numerator_strength": "1"
}

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