Label: MCKESSON COUGH SUPRESSANT- menthol lozenge
- NDC Code(s): 68599-0500-3
- Packager: McKesson Medical-Surgical
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 5, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
MCKESSON COUGH SUPRESSANT
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68599-0500 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 7.6 mg Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662) FD&C RED NO. 40 (UNII: WZB9127XOA) SUCROSE (UNII: C151H8M554) CORN SYRUP (UNII: 9G5L16BK6N) Product Characteristics Color red Score no score Shape OVAL Size 22mm Flavor CHERRY Imprint Code P Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68599-0500-3 300 in 1 CARTON; Type 0: Not a Combination Product 05/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 05/02/2022 Labeler - McKesson Medical-Surgical (023904428) Registrant - Unifirst First Aid Corporation (832947092)