COUGH DROPS FREEGELLS STRAWBERRY 30CT- menthol lozenge 
R.L. ALBERT & SON, 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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Drug Facts

Active ingredient

 Menthol 2.7 mg

Purpose

Cough Suppressant / Oral anesthetic

Use

Temporarily relieves:

Warning

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

dissolve 2 lozenges (one at a time) slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor

children under 5 years , ask a doctor 

Other information

Inactive ingredients

Beta Carotene (color), corn syrup, eucalyptus oil, honey, natural & artificial flavors, soy lecithin, sucrose and water

Product label

image descriptionimage description

COUGH DROPS FREEGELLS STRAWBERRY 30CT 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83002-010
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.7 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
CORN SYRUP (UNII: 9G5L16BK6N)  
EUCALYPTOL (UNII: RV6J6604TK)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Product Characteristics
ColorredScoreno score
ShapeOVALSize20mm
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83002-010-019 in 1 CARTON07/14/2023
130 in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/14/2023
Labeler - R.L. ALBERT & SON, INC (005900899)

Revised: 7/2023
Document Id: 00b08b8a-44c7-0238-e063-6394a90a5047
Set id: dc077c36-c403-4b83-894a-e9922e928841
Version: 1
Effective Time: 20230717
 
R.L. ALBERT & SON, INC