Dermveda ULTRA BITE ITCH RELIEF

UNIISPL

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

Identification

ManufacturerCelcius Corp.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8381910602
60 mL in 1 JAR (83819-106-02)

Annotations

UNII (FDA Substance ID)

79M2M2UDA9

MENTHA X PIPERITA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "79M2M2UDA9",
    "rxcui": null,
    "inchikey": null,
    "display_name": "MENTHA X PIPERITA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "f43bc300-50bf-421a-81f8-1da7fc829cd0": {
      "match": "brand_token",
      "title": "DERMVEDA ULTRA FOLLICULITIS TREATMENT (SULFUR, CURCUMA LONGA) CREAM [CELCIUS CORP.]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "83819-106_f0ecbd75-2453-42c5-9ca7-03a3a6fabe65",
  "productndc": "83819-106",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHA X PIPERITA WHOLE; TURMERIC",
  "proprietary_name": "Dermveda ULTRA BITE ITCH RELIEF",
  "active_ingred_unit": "[hp_X]/60mL; [hp_C]/60mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Mentha Piperita, Curcuma Longa",
  "start_marketing_date": "20240918",
  "active_numerator_strength": "10; 10"
}

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