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Listerine Ultraclean Antiseptic

NDC 69968-0788 · Kenvue Brands LLC

Generic nameEucalyptol, Menthol, Methyl Salicylate, Thymol
Dosage formMOUTHWASH
RouteORAL
Active ingredient(s)THYMOL, EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE
Strength.92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

69968-0788-1 — 1000 mL in 1 BOTTLE, PLASTIC (69968-0788-1)

69968-0788-2 — 1500 mL in 1 BOTTLE, PLASTIC (69968-0788-2)

69968-0788-5 — 500 mL in 1 BOTTLE, PLASTIC (69968-0788-5)

69968-0788-9 — 2 BOTTLE, PLASTIC in 1 PACKAGE (69968-0788-9) / 1500 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-693 — Benzocaine, 69892-072 — Eucalyptol, Menthol, Methyl salicylate, Thymol, 69892-664 — Eucalyptol, menthol, methyl salicylate, thymol, 69968-0239 — Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol, 69968-0400 — Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol, 69968-0487 — Menthol, Unspecified Form, 69968-0538 — CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, and Methyl Salicylate, 69968-0539 — Eucalyptol, Menthol, unspecified form, Methyl Salicylate, and Thymol, 69968-0550 — Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol, 69968-0595 — MENTHOL, UNSPECIFIED FORM, 69968-0790 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0791 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0792 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0793 — Lidocaine, Menthol, 69968-0818 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0948 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0949 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0955 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 69968-0959 — Eucalyptol, Menthol, Methyl Salicylate, Thymol, 70000-0208 — Camphor (Synthetic), Menthol, Unspecified Form, and Methyl Salicylate, +847 more

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