United States · FDA National Drug Code directory
Biofreeze
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
- 59316-101_51b434c9-228b-2c05-e063-6394a90a1e94
- Product NDC
- 59316-101
- Form
- GEL
- Composition / generic term
- Menthol
- Labeler
- Reckitt Benckiser LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20160825
- Source listing expiry
- 20271231
Source-listed ingredients
- MENTHOL, UNSPECIFIED FORM — 35 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 mL in 1 PACKET (59316-101-10) · 59316-101-10
- 30 mL in 1 BOTTLE (59316-101-11) · 59316-101-11
- 59 mL in 1 TUBE (59316-101-12) · 59316-101-12
- 59 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-13) · 59316-101-13
- 89 mL in 1 BOTTLE, WITH APPLICATOR (59316-101-15) · 59316-101-15
- 3 mL in 1 PACKET (59316-101-19) · 59316-101-19
- 118 mL in 1 TUBE (59316-101-20) · 59316-101-20
- 473 mL in 1 BOTTLE, PUMP (59316-101-30) · 59316-101-30
- 946 mL in 1 BOTTLE, PUMP (59316-101-40) · 59316-101-40
- 3785 mL in 1 BOTTLE, PUMP (59316-101-50) · 59316-101-50
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 →