Label: MEIJER SEVERE MENTHOL THROAT DROPS- menthol lozenge
- NDC Code(s): 79481-0092-1
- Packager: Meijer
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
MEIJER SEVERE MENTHOL THROAT DROPS
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0092 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 20 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color white (White with blue flakes) Score no score Shape OVAL Size 17mm Flavor MENTHOL Imprint Code B Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0092-1 45 in 1 BAG; Type 0: Not a Combination Product 04/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/18/2024 Labeler - Meijer (006959555) Registrant - Bestco (002149136) Establishment Name Address ID/FEI Business Operations Bestco 002149136 manufacture(79481-0092)