CHERRY COUGH DROP- menthol lozenge 
BestCo Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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:

When using this product

do not exceed recommended dosage

Stop use and consult 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 two hours as necessary or as directed by a dcotro

children under 5 years ask a doctor

Other information

Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C red no. 40, glycerin, medium chain triglycerides, natural and artificial flavors, soybean oil, sucrose and water.

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

BestHealth Cherry 200ct Cough Drops

CHERRY COUGH DROP 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52642-012
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
ColorredScorescore with uneven pieces
ShapeOVALSize17mm
FlavorCHERRYImprint Code B
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52642-012-00200 in 1 BAG; Type 0: Not a Combination Product04/27/2015
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34104/27/2015
Labeler - BestCo Inc. (002149136)
Registrant - BestCo Inc. (002149136)
Establishment
NameAddressID/FEIBusiness Operations
BestCo Inc.002149136manufacture(52642-012)

Revised: 10/2023
Document Id: 06e76e24-a425-5ffd-e063-6294a90a4911
Set id: 4bceb540-5a0d-0167-e054-00144ff8d46c
Version: 5
Effective Time: 20231004
 
BestCo Inc.