GREEN GUARD COUGH DROP RELIEF- 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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Green Guard Cough Drop Relief

Drug Facts

Active ingredient (in each drop)

Menthol 7.6 mg

Purpose

Anititussive (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, 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

■ cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent
headache. These could be signs of a serious condition.

■ sore mouth does not improve in 7 days

■ irritation, pain, or redness persists or worsens

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

cherry flavor, corn syrup, eucalyptus oil, FD&C red #40, sucrose

Questions or comments? 1-800-869-6970

Green Guard Cough Drop Label

Green Guard Cough Drop Relief Label

Medicated Cherry

Cough Drop relief

Green Guard ®

Pull To Open

Tire Para Abrir

Menthol 7.6mg

Mentol 7.6mg

Cough Supressant/Anethetic

Suprime la tos/anestesico

125 Drops

Order #2242

Distributed by Green Guard®, St Louis, MO 63045

GG Cherry

GREEN GUARD COUGH DROP RELIEF 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-018
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL7.6 mg
Inactive Ingredients
Ingredient NameStrength
CORN SYRUP (UNII: 9G5L16BK6N)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Colorred (red) Scoreno score
ShapeOVAL (OVAL) Size22mm
FlavorCHERRY (Cherry) Imprint Code P
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-018-5050 in 1 BOX; Type 0: Not a Combination Product11/01/2011
2NDC:47682-018-25125 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)

Revised: 3/2022
Document Id: da456b1e-c70b-984f-e053-2a95a90a3753
Set id: 0fc4cb11-8ff9-4eff-9588-c73eef4e0137
Version: 10
Effective Time: 20220315
 
Unifirst First Aid Corporation