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United States · US · US:59316-001_51b57c01-885b-f5b1-e063-6294a90a75e9

Biofreeze Foot Cream

UNIISPL

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

Identification

ManufacturerReckitt Benckiser LLC
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    5931600110
    85 g in 1 TUBE (59316-001-10)
  • ndc11
    5931600120
    113.3 g in 1 TUBE (59316-001-20)

Annotations

UNII (FDA Substance ID)
L7T10EIP3A
MENTHOL, UNSPECIFIED FORM
RxCUI 6750
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "L7T10EIP3A",
    "rxcui": "6750",
    "inchikey": null,
    "display_name": "MENTHOL, UNSPECIFIED FORM",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "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": "59316-001_51b57c01-885b-f5b1-e063-6294a90a75e9",
  "productndc": "59316-001",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Biofreeze Foot Cream",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20210312",
  "active_numerator_strength": "100"
}

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