Biofreeze Colorless Roll-On

UNIISPL

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

Identification

ManufacturerReckitt Benckiser LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5931620610
1 BOTTLE, WITH APPLICATOR in 1 CARTON (59316-206-10) / 89 mL in 1 BOTTLE, WITH APPLICATOR

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": "59316-206_51b58e7e-a6c1-b40f-e063-6394a90a1f1e",
  "productndc": "59316-206",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Biofreeze Colorless Roll-On",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20130117",
  "active_numerator_strength": "40"
}

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