United States · FDA National Drug Code directory

Biofreeze Professional Roll-On

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
59316-117_51e09cee-5dd5-65f6-e063-6394a90a2c67
Product NDC
59316-117
Form
GEL
Composition / generic term
MENTHOL, UNSPECIFIED FORM
Labeler
Reckitt Benckiser LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20160603
Source listing expiry
20271231

Source-listed ingredients

  • MENTHOL, UNSPECIFIED FORM — 50 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 89 mL in 1 BOTTLE (59316-117-10) · 59316-117-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →