Label: EQUATE SEVERE MENTHOL THROAT DROP- menthol lozenge
- NDC Code(s): 79903-254-45
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 27, 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
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE SEVERE MENTHOL THROAT DROP
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-254 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 (Translucent to 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:79903-254-45 45 in 1 BAG; Type 0: Not a Combination Product 02/27/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 02/27/2024 Labeler - Walmart (051957769) Registrant - Bestco (002149136) Establishment Name Address ID/FEI Business Operations Bestco 002149136 manufacture(79903-254)