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United States Β· US Β· US:59316-207_51e06d5e-11fe-5814-e063-6294a90a2736

Biofreeze Overnight Roll-on

SPL

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

Identification

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

Packs Β· 1

  • ndc11
    5931620714
    74 mL in 1 BOTTLE (59316-207-14)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "TOPICAL",
  "spl_meta": {
    "71a36691-9d9e-479d-bfdc-6f6b192ad2d0": {
      "match": "brand_token",
      "title": "BIOFREEZE MENTHOL (MENTHOL, UNSPECIFIED FORM) PATCH [RECKITT BENCKISER LLC]",
      "spl_version": "4",
      "published_date": "2026-05-28"
    }
  },
  "productid": "59316-207_51e06d5e-11fe-5814-e063-6294a90a2736",
  "productndc": "59316-207",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "Biofreeze Overnight Roll-on",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20230316",
  "active_numerator_strength": "40"
}

Access this data programmatically

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Biofreeze Overnight Roll-on (US) β€” Drug Database