United States · FDA National Drug Code directory
Biofreeze Menthol
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
- 59316-887_51b56b5f-5a3c-cc70-e063-6294a90a4580
- Product NDC
- 59316-887
- Form
- KIT
- Composition / generic term
- Menthol, Unspecified form
- Labeler
- Reckitt Benckiser LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20220310
- Source listing expiry
- 20271231
Source-listed ingredients
Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.
These values do not establish equivalence or a dose recommendation.
Packages
- 1 KIT in 1 KIT (59316-887-04) * 1 PATCH in 1 POUCH (59316-992-32) / 20 g in 1 PATCH * 1 PATCH in 1 POUCH (59316-992-33) / 13 g in 1 PATCH · 59316-887-04
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 →