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United States Β· US Β· US:87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386

BENOVA PAIN AND ITCH RELIEF

SPL

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

Identification

ManufacturerBENOVA RX LLC
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    8715000103
    90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "TOPICAL",
  "spl_meta": {
    "42513ee2-8b40-a9f3-e063-6394a90a9386": {
      "match": "brand_token",
      "title": "BENOVA PAIN AND ITCH RELIEF (MENTHOL, 0.11%) LOTION [BENOVA RX LLC]",
      "spl_version": "1",
      "published_date": "2025-12-15"
    }
  },
  "productid": "87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386",
  "productndc": "87150-001",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "BENOVA PAIN AND ITCH RELIEF",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, 0.11%",
  "start_marketing_date": "20251215",
  "active_numerator_strength": "1.1"
}

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BENOVA PAIN AND ITCH RELIEF (US) β€” Drug Database