Label: GREEN GUARD COUGH DROP RELIEF- menthol lozenge
- NDC Code(s): 47682-018-25, 47682-018-50
- Packager: Unifirst First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.
Ask a doctor before use if you have
■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema
■ cough accompanied by excessive phlegm (mucus)
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- QUESTIONS
- Green Guard Cough Drop Label
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INGREDIENTS AND APPEARANCE
GREEN GUARD COUGH DROP RELIEF
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-018 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 (red) Score no score Shape OVAL (OVAL) Size 22mm Flavor CHERRY (Cherry) Imprint Code P Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-018-50 50 in 1 BOX; Type 0: Not a Combination Product 11/01/2011 2 NDC:47682-018-25 125 in 1 BOX; Type 0: Not a Combination Product 11/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 11/01/2011 Labeler - Unifirst First Aid Corporation (832947092)