United States · FDA National Drug Code directory
Biofreeze Professional Colorless 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
- 59316-118_51993a5e-b316-10ee-e063-6294a90a4d72
- Product NDC
- 59316-118
- 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
- 74 mL in 1 BOTTLE (59316-118-05) · 59316-118-05
- 89 mL in 1 BOTTLE (59316-118-10) · 59316-118-10
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 →