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United States · US · US:11673-842_58c5a8ee-8dd7-4bf6-a793-164a67fa9c33

up and up hydrocortisone anti itch

UNIISPLATC A07EA02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerTarget Corporation
CountryUS (United States)
ATC codeA07EA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1167384200
    2 TUBE in 1 CARTON (11673-842-00) / 56 g in 1 TUBE

Annotations

UNII (FDA Substance ID)
WI4X0X7BPJ
HYDROCORTISONE
RxCUI 5492
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "WI4X0X7BPJ",
    "rxcui": "5492",
    "inchikey": "JYGXADMDTFJGBT-VWUMJDOOSA-N",
    "display_name": "HYDROCORTISONE",
    "substance_type": "chemical",
    "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": "11673-842_58c5a8ee-8dd7-4bf6-a793-164a67fa9c33",
  "productndc": "11673-842",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYDROCORTISONE",
  "proprietary_name": "up and up hydrocortisone anti itch",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "hydrocortisone",
  "start_marketing_date": "20200214",
  "active_numerator_strength": "1"
}

Related drugs

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