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MENTHOL

NDC 72937-632 · SUNSET PAIN RELIEF

Generic nameMENTHOL
Dosage formGEL
RouteTOPICAL
Active ingredient(s)MENTHOL, UNSPECIFIED FORM
Strength4 g/100mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

72937-632-03 — 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72793-100 — Menthol, 72793-200 — Menthol, Camphor, 72793-201 — Menthol, 72854-265 — BENZOCAINE and Menthol, Unspecified Form, 72863-076 — CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM, 72937-004 — MENTHOL, 72937-010 — MENTHOL, CAMPHOR, 72937-022 — MENTHOL, CAMPHOR, 72937-300 — MENTHOL, CAMPHOR, 72937-627 — MENTHOL, CAMPHOR, 73132-001 — Camphor, Menthol, Methyl Salicylate, 73132-003 — Menthol, 73132-005 — Menthol, 73352-575 — menthol, unspecified form and methyl salicylate, 73598-1202 — MENTHOL, UNSPECIFIED FORM, 73598-1204 — MENTHOL, UNSPECIFIED FORM, 73635-5802 — Menthol 1%, 73647-103 — MENTHOL, CAMPHOR, 73647-310 — MENTHOL, CAMPHOR, 75568-041 — MENTHOL, UNSPECIFIED FORM, +380 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels