United States · FDA National Drug Code directory
Biofreeze 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
- 59316-205_51e07cc8-7357-2dce-e063-6394a90af835
- Product NDC
- 59316-205
- Form
- GEL
- Composition / generic term
- MENTHOL
- Labeler
- Reckitt Benckiser LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20130117
- Source listing expiry
- 20271231
Source-listed ingredients
- MENTHOL, UNSPECIFIED FORM — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 37 mL in 1 BOTTLE (59316-205-09) · 59316-205-09
- 89 mL in 1 BOTTLE (59316-205-10) · 59316-205-10
- 74 mL in 1 BOTTLE (59316-205-14) · 59316-205-14
- 2 BOTTLE in 1 CARTON (59316-205-81) / 89 mL in 1 BOTTLE (59316-205-10) · 59316-205-81
- 2 BOTTLE in 1 CARTON (59316-205-82) / 89 mL in 1 BOTTLE (59316-205-10) · 59316-205-82
Source and coverage
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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.
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