Biofreeze Professional

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 · 6

ndc11
5931611511
3 mL in 1 PACKET (59316-115-11)
ndc11
5931611520
118 mL in 1 TUBE (59316-115-20)
ndc11
5931611530
473 mL in 1 BOTTLE (59316-115-30)
ndc11
5931611540
946 mL in 1 BOTTLE (59316-115-40)
ndc11
5931611550
3785 mL in 1 BOTTLE (59316-115-50)
ndc11
5931611582
100 PACKET in 1 CARTON (59316-115-82) / 3 mL in 1 PACKET

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": "59316-115_51e07a73-db68-3e69-e063-6394a90a6bdb",
  "productndc": "59316-115",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Biofreeze Professional",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, UNSPECIFIED FORM",
  "start_marketing_date": "20160603",
  "active_numerator_strength": "50"
}

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