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Coralite Ultra Strength Pain Relief

NDC 65923-532 · United Exchange Corp.

Generic nameCamphor Menthol

Dosage formOINTMENT

RouteTOPICAL

Active ingredient(s)CAMPHOR (SYNTHETIC), MENTHOL

Strength110; 110 mg/g; mg/g

Marketing categoryOTC MONOGRAPH DRUG

Packages

65923-532-18 — 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65282-1815 — alcohol, menthol, and benzocaine prep pad, 65753-400 — camphor, diphenhydramine, zinc acetate, 65852-015 — Benzocaine, Menthol, Zinc chloride, 65923-104 — Menthol, 65923-121 — Menthol, 65923-122 — Menthol, 65923-146 — Menthol and Capsaicin, 65923-148 — Camphor, Menthol, and Mehtyl salicylate, 65923-205 — Menthol, 65923-214 — Menthol, 65923-564 — Camphor, Menthol, Methyl Salicylate, 65923-987 — Camphor, Menthol, and Methyl Salicylate, 66059-0005 — Camphor, Menthol, 66506-184 — Menthol, 66761-129 — METHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, and CAMPHOR (SYNTHETIC), 66761-130 — METHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, and CAMPHOR (SYNTHETIC), 66761-308 — Camphor (Synthetic) and Menthol, 66761-309 — Camphor (Synthetic) and Menthol, 66761-315 — Camphor (Synthetic) and Menthol, 66761-322 — Camphor (Synthetic), Menthol, and Capsicum, +2023 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.