SEVERE THROAT SORE DROPS- menthol pastille 
Target Corporation 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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Severe Throat Drops Oral Anesthetic

Active Ingredient in each drop Purposes

Menthol 20mg Cough Suppressant

Oral anesthetic

Temporarily relieves ocassional minor irritation and pain due to:

Temporarily relieves ocassional minor irritation and pain due to:

Warnings

Sore throat warning: severe or persistence sore throat accompanied or followed by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

Ask a doctor before use if you have

Stop use and consult 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.

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Directions

eucalyptus oil, FD&C Blue No.1, glucose syrup, gum arabic, sucrose

Back Label

Questions? or to report and adverse event call: 1-617-848-4560

Monday to Friday 9AM to 4 PM east

Front Label

SEVERE THROAT SORE DROPS 
menthol pastille
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-143
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.69 mg
Inactive Ingredients
Ingredient NameStrength
EUCALYPTUS OIL (UNII: 2R04ONI662)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
ACACIA (UNII: 5C5403N26O)  
SUCROSE (UNII: C151H8M554)  
CORN SYRUP (UNII: 9G5L16BK6N)  
Product Characteristics
Colorwhite (with menthol drops) Scorescore with uneven pieces
ShapeRECTANGLESize17mm
FlavorMENTHOLImprint Code None
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-143-0145 in 1 BAG; Type 0: Not a Combination Product10/12/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/12/2019
Labeler - Target Corporation Inc. (006961700)
Registrant - Boston Nutraceutical Science SL (466061824)
Establishment
NameAddressID/FEIBusiness Operations
Boston Nutraceutical Production SL468121064manufacture(11673-143) , label(11673-143) , pack(11673-143)

Revised: 1/2023
Document Id: f1ebcae5-9ef7-8112-e053-2a95a90a44cd
Set id: 949543d5-5043-ac06-e053-2995a90ab398
Version: 2
Effective Time: 20230110
 
Target Corporation Inc.