Label: CHERRY COUGH DROPS- menthol lozenge
- NDC Code(s): 52642-043-40
- Packager: Bestco Inc.
- Category: HUMAN OTC DRUG LABEL
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Updated December 27, 2019
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
CHERRY COUGH DROPS
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52642-043 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5.8 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color red Score no score Shape OVAL Size 17mm Flavor CHERRY Imprint Code B Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52642-043-40 40 in 1 BAG; Type 0: Not a Combination Product 10/10/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 10/10/2018 Labeler - Bestco Inc. (002149136) Registrant - Bestco Inc. (002149136) Establishment Name Address ID/FEI Business Operations Bestco Inc. 002149136 manufacture(52642-043)