DERMOSCRIBE SEBORRHEIC DERMATITIS

UNIISPLATC D07AB

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

Identification

ManufacturerDERMOSCRIBE PTY LTD

CountryUS (United States)

ATC codeD07AB

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6968320211
60 g in 1 BOTTLE (69683-202-11)

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": {
    "2b6bf90b-5d42-4c08-afee-56e13122285e": {
      "match": "brand_token",
      "title": "DERMOSCRIBE SEBORRHEIC DERMATITIS (SULFUR, SALICYLIC ACID, HYDROCORTISONE) CREAM [DERMOSCRIBE PTY LTD]",
      "spl_version": "9",
      "published_date": "2025-11-17"
    }
  },
  "productid": "69683-202_4161aee0-5f36-1739-e063-6294a90a5bdf",
  "productndc": "69683-202",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYDROCORTISONE; SALICYLIC ACID; SULFUR",
  "proprietary_name": "DERMOSCRIBE SEBORRHEIC DERMATITIS",
  "active_ingred_unit": "g/100g; g/100g; g/100g",
  "application_number": "M032",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "SULFUR, SALICYLIC ACID, HYDROCORTISONE",
  "start_marketing_date": "20150323",
  "active_numerator_strength": "1; 3; 3"
}

Related drugs

Other records sharing ATC code D07AB.

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