FREEGELLS COUGH DROPS HONEY LEMON 200CT- menthol lozenge 
RL Albert & Son Inc.

----------

Drug Facts

Active ingredient (in each drop)

Menthol 7.5 mg

Purpose

Cough suppressant/Oral anesthetic

Uses

Temporarily relieves:

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 a 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 1 lozenge 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 description

FREEGELLS COUGH DROPS HONEY LEMON 200CT 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83002-043
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL7.5 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
CORN SYRUP (UNII: 9G5L16BK6N)  
EUCALYPTOL (UNII: RV6J6604TK)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
APIS MELLIFERA (UNII: 7S82P3R43Z)  
BETA CAROTENE (UNII: 01YAE03M7J)  
Product Characteristics
ColoryellowScoreno score
ShapeOVALSize20mm
FlavorHONEY (Lemon) Imprint Code F
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83002-043-014 in 1 CARTON03/15/2024
1200 in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/15/2024
Labeler - RL Albert & Son Inc. (005900899)

Revised: 4/2024
Document Id: 16641a1b-f631-484b-e063-6294a90ae411
Set id: 3ac08274-08d9-4dab-b09a-6e297948a25a
Version: 1
Effective Time: 20240418
 
RL Albert & Son Inc.