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United States · US · US:10738-059_497d62b9-309b-5d55-e063-6294a90a7e41

TRIDERMA EVERYDAY BRUISE RELIEF

SPL

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

Identification

ManufacturerGenuine Virgin Aloe Corporation
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    1073805920
    1 TUBE in 1 CARTON (10738-059-20) / 62 g in 1 TUBE (10738-059-25)
  • ndc11
    1073805941
    113 g in 1 JAR (10738-059-41)
  • ndc11
    1073805950
    1 TUBE in 1 CARTON (10738-059-50) / 14 g in 1 TUBE (10738-059-55)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "TOPICAL",
  "spl_meta": {
    "1f11fe3f-487b-4e31-8cdd-2d93560c665f": {
      "match": "brand_token",
      "title": "TRIDERMA STUBBORN ECZEMA ITCH RELIEF (STUBBORN E RELIEF) CREAM [GENUINE VIRGIN ALOE CORPORATION]",
      "spl_version": "1",
      "published_date": "2026-02-02"
    }
  },
  "productid": "10738-059_497d62b9-309b-5d55-e063-6294a90a7e41",
  "productndc": "10738-059",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ARNICA MONTANA",
  "proprietary_name": "TRIDERMA EVERYDAY BRUISE RELIEF",
  "active_ingred_unit": "g/100g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ARNICA MONTANA",
  "start_marketing_date": "20190830",
  "active_numerator_strength": "1.6"
}

Access this data programmatically

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