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NATURAL LEMON MINT HERB THROAT DROPS

Dosage form: lozenge
Ingredients: MENTHOL 1.6mg
Labeler: Ricola USA Inc.
NDC Code: 63667-676

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.

NATURAL LEMON MINT HERB THROAT DROPS

Drug Facts

Purpose

Oral pain reliever

Active Ingredient (in each drop)

Menthol, 1.6 mg

Uses

temporarily relieves occasional minor irritation and pain associated with:

  • sore mouth
  • sore throat

Warnings

Do not use

  • in children under 6 years of age unless directed by a doctor.

Stop use and ask a doctor if
  • sore throat is severe, persists for more than 2 days, or is accompanied by fever, headache, rash, nausea or vomiting.
  • sore mouth symptoms do not improve in 7 days.

Keep out of reach of children.


Directions
  • adults and children 6 years and older:  dissolve 2 drops (one at a time) slowly in the mouth.  Repeat every 2 hours as needed or as directed by a doctor
  • children under 6 years: ask a doctor

Inactive Ingredients

citric acid, extracts of lemon balm and a Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), natural color (beta carotene), natural flavors, starch syrup, sugar

NATURAL LEMON MINT HERB THROAT DROPS 
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63667-676
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL1.6 mg
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
SUCROSE 
Product Characteristics
Coloryellow (GOLDEN YELLOW) Scoreno score
ShapeOVALSize24mm
FlavorLEMON (LEMON MINT) Imprint CodeR
Contains    
Packaging
#Item CodePackage Description
1NDC:63667-676-1010 LOZENGE in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35601/01/1942
Labeler - Ricola USA Inc. (177265261)
Establishment
NameAddressID/FEIOperations
Ricola Ag480227248manufacture(63667-676)

Revised: 12/2017
 
Ricola USA Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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