up and up medicated wipes

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 · 2

ndc11
1167340448
48 APPLICATOR in 1 CELLO PACK (11673-404-48) / 5.375 g in 1 APPLICATOR
ndc11
1167340496
2 CELLO PACK in 1 CARTON (11673-404-96) / 48 APPLICATOR in 1 CELLO PACK / 5.375 g in 1 APPLICATOR

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": {
    "51c0a953-93cb-4d0a-b51c-02d9482d1746": {
      "match": "brand_token",
      "title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
      "spl_version": "12",
      "published_date": "2026-05-13"
    }
  },
  "productid": "11673-404_265bc6e5-458e-68bd-e063-6394a90aed53",
  "productndc": "11673-404",
  "dosage_form": "SWAB",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "up and up medicated wipes",
  "active_ingred_unit": "g/g",
  "application_number": "M015",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "gentle hemorrhoidal care",
  "start_marketing_date": "20150101",
  "active_numerator_strength": ".5"
}

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