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United States · US · US:85248-181_4eee7637-3a29-e0bd-e063-6294a90ae1a4

DRMITSUI ECZEMA RELIEF

UNIISPLATC A07EA02

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

Identification

ManufacturerJiangxi Yudexi Pharmaceutical Co., LTD
CountryUS (United States)
ATC codeA07EA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8524818101
    20 g in 1 TUBE (85248-181-01)

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": {
    "4f3e83a7-ebc9-76e7-e063-6394a90a9e9e": {
      "match": "brand_token",
      "title": "DRMITSUI VAGINAL PROBIOTICS (VAGINAL PROBIOTICS) GEL [GUANGZHOU ZHUOYUE TRADING CO., LTD]",
      "spl_version": "1",
      "published_date": "2026-05-11"
    }
  },
  "productid": "85248-181_4eee7637-3a29-e0bd-e063-6294a90ae1a4",
  "productndc": "85248-181",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYDROCORTISONE",
  "proprietary_name": "DRMITSUI ECZEMA RELIEF",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Hydrocortisone 1% ECZEMA RELIEF",
  "start_marketing_date": "20260408",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A07EA02.

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