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TRIDERMA PAIN RELIEF

NDC 10738-073 · Genuine Virgin Aloe Corporation

Generic nameLidocaine HCl, Menthol

Dosage formCREAM

RouteTOPICAL

Active ingredient(s)LIDOCAINE HYDROCHLORIDE, MENTHOL, UNSPECIFIED FORM

Strength4; 1 g/100g; g/100g

Pharmacologic classAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]

Marketing categoryOTC MONOGRAPH DRUG

Packages

10738-073-21 — 57 g in 1 JAR (10738-073-21)

10738-073-41 — 113 g in 1 JAR (10738-073-41)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10157-9913 — camphor (synthetic), dimethicone, unspecified, menthol, unspecified form, and phenol, 10157-9951 — Dimethicone, Camphor (synthetic), Menthol, and Phenol, 10237-760 — Hydrogen Peroxide and Menthol, 10237-784 — Hydrogen peroxide, Menthol, 10237-787 — Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride, 10237-788 — Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride, 10237-789 — Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride, 10237-792 — benzocaine, menthol, zinc chloride, 10237-796 — Benzocaine and Menthol, 10237-799 — Menthol and Hydrogen Peroxide, 10742-0002 — camphor, menthol, 10742-1117 — Menthol, 10742-1118 — Menthol, 10742-1389 — Lidocaine HCl, Menthol, 10742-2002 — menthol, methyl salicylate, 10742-2112 — camphor, eucalyptus oil, menthol, 10742-6000 — Camphor, Menthol, Methyl salicylate, 10742-8096 — camphor, eucalyptus oil, menthol, 10742-8125 — menthol, 10742-8168 — camphor, eucalyptus oil, menthol, +1090 more

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