United States · FDA National Drug Code directory
Coralite Ultra Strength Pain Relief
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
- 65923-532_425530d6-e8ea-f05c-e063-6294a90aff39
- Product NDC
- 65923-532
- Form
- OINTMENT
- Composition / generic term
- Camphor Menthol
- Labeler
- United Exchange Corp.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20141015
- Source listing expiry
- 20261231
Source-listed ingredients
- CAMPHOR (SYNTHETIC) — 110 mg/g
- MENTHOL — 110 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR · 65923-532-18
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 →