BIOFREEZE

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 · 11

ndc11
5931610210
5 mL in 1 BOTTLE (59316-102-10)
ndc11
5931610211
3 mL in 1 BOTTLE (59316-102-11)
ndc11
5931610212
89 mL in 1 BOTTLE (59316-102-12)
ndc11
5931610220
118 mL in 1 BOTTLE (59316-102-20)
ndc11
5931610228
237 mL in 1 BOTTLE (59316-102-28)
ndc11
5931610230
473 mL in 1 BOTTLE (59316-102-30)
ndc11
5931610240
946 mL in 1 BOTTLE (59316-102-40)
ndc11
5931610250
3785 mL in 1 CONTAINER (59316-102-50)
ndc11
5931610280
44 mL in 1 TUBE (59316-102-80)
ndc11
5931610290
100 BOTTLE in 1 CARTON (59316-102-90) / 5 mL in 1 BOTTLE (59316-102-10)
ndc11
5931610298
30 mL in 1 BOTTLE (59316-102-98)

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": "59316-102_51b44481-a7ad-8a46-e063-6294a90aefda",
  "productndc": "59316-102",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "BIOFREEZE",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20120103",
  "active_numerator_strength": "40"
}

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