MEDIQUE SUGAR FREE MEDIKOFF DROPS- menthol lozenge 
Unifirst First Aid Corporation

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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MEDIQUE SUGAR FREE MEDIKOFF DROPS

Drug Facts

Active ingredient (in each drop)

Menthol 5.8 mg

Purpose

Antitussive (cough suppressant)/oral anesthetic

Uses

temporarily relieves

■ cough as may occur with a cold or inhaled irritants

■ 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, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.

Ask a doctor before use if you have

  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if

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

Keep this and all drugs out of the reach of children.

Directions

​Adults and Children (12 years and older)

​Allow 1 drop to dissolve slowly in the mouth. May be repeated every 2 hours as necessary or as directed by a doctor.

Children under 12 years: Ask a doctor

Other information

Inactive ingredients

acesulfame potassium, eucalyptus oil, flavoring, isomalt

Questions or comments? 1-800-634-7680

Medique Medikoff Sugar Free

Medique ®

Sugar Free Medikoff Drops

Vapor Action with Eucalyptus

Accion Vaporizante con Eucalypto

Cough Supressant/Anesthetic • Menthol 5.8mg

Suprima la tos/anestesico • Mentol 5.8 mg

Pull to Open

Tire Para Abrir

300 Lozenges

300 Pastillas

Individually Wrapped Cough Drops

Individualmento envuelto pastillas para la tos

Collect MediBucks

See inside flap for more details

109R MedikoffSFree

MEDIQUE SUGAR FREE MEDIKOFF DROPS 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-110
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5.8 mg
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
ISOMALT (UNII: S870P55O2W)  
Product Characteristics
Colorwhite (translucent) Scoreno score
ShapeOVAL (OVAL) Size23mm
FlavorImprint Code P
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-110-03300 in 1 BOX; Type 0: Not a Combination Product11/01/2011
2NDC:47682-110-055 in 1 BOX; Type 0: Not a Combination Product11/01/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34111/01/2011
Labeler - Unifirst First Aid Corporation (832947092)
Registrant - Unifirst First Aid Corporation (832947092)

Revised: 3/2023
Document Id: f7a5b544-e21d-e6cf-e053-6294a90a681c
Set id: 92d13e19-4e7b-4565-970e-504abf02579a
Version: 13
Effective Time: 20230324
 
Unifirst First Aid Corporation