CHERRY COUGH DROPS- menthol lozenge 
American Sales

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Menthol 5.8 mg

Active ingredient (in each drop)

Menthol 5.8 mg

Purpose

Cough suppressant / Oral anesthetic

Uses temporarily relieves:

cough as may occur with a cold

occasional minor irritation and sore throat

Warnings

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 a doctor before use if you have:

Stop use and ask doctor if

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

adults and children 5 years and over - allow 1 drop to dissolve slowly in mouth. May be repeated every 2 hours as necessary or as directed by a doctor.

children under 5 years - ask a doctor

Other information

Inactive ingredients: Acesulfame potassium (non-nutritive sweetener), corn starch, eucalyptus oil, FD&C blue no. 1, FD&C red no. 40, glycerin, isomalt, maltitol syrup, medium chain triglycerides, natural and artificial flavors, soybean oil, sucralose (non-nutritive sweetener) and water.

Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST

CareOne SF Cherry 25ct Cough Drops

CHERRY COUGH DROPS 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-044
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5.8 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorred (maroon) Scoreno score
ShapeOVALSize16mm
FlavorCHERRYImprint Code B
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41520-044-2525 in 1 BAG; Type 0: Not a Combination Product06/22/2016
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/22/2016
Labeler - American Sales (809183973)
Registrant - Bestco Inc. (002149136)
Establishment
NameAddressID/FEIBusiness Operations
Bestco Inc.002149136manufacture(41520-044)

Revised: 1/2024
Document Id: 0e87aa19-bbe5-d384-e063-6294a90a9d0b
Set id: 48961fbb-7ff0-4c24-e054-00144ff8d46c
Version: 7
Effective Time: 20240109
 
American Sales