Biofreeze 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 · 5

ndc11
5931620509
37 mL in 1 BOTTLE (59316-205-09)
ndc11
5931620510
89 mL in 1 BOTTLE (59316-205-10)
ndc11
5931620514
74 mL in 1 BOTTLE (59316-205-14)
ndc11
5931620581
2 BOTTLE in 1 CARTON (59316-205-81) / 89 mL in 1 BOTTLE (59316-205-10)
ndc11
5931620582
2 BOTTLE in 1 CARTON (59316-205-82) / 89 mL in 1 BOTTLE (59316-205-10)

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": "59316-205_51e07cc8-7357-2dce-e063-6394a90af835",
  "productndc": "59316-205",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Biofreeze 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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