Herbal Throat Drops

Manufacturer
Meijer, Inc. | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
Effective date
2025-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:24

Label at a glance#

ProductHerbal Throat Drops
Active ingredientMENTHOL
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

  • Menthol 1.1 mg

Front labelFront label

OTC - PURPOSE SECTION

Uses temporarily relieves:

ocassional minor irritation and pain associated with

  • sore mouth
  • sore throat

INDICATIONS & USAGE SECTION

Uses temporarily relieves:
ocassional minor irritation and pain associated with

  • sore mouth
  • sore throat

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

Stop and consult a doctor if

  • sore throat is severe, or irritation, pain or redness last or worsens.
  • sore mouth does not improve in 7 days.

OTC - STOP USE SECTION

Stop and consult a doctor if

  • sore throat is severe, or irritation, pain or redness last or worsens.
  • sore mouth does not improve in 7 days.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OVERDOSAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 6 years and over: dissolve 1 drop slowly in mouth. Repeated every 2 hours as needed or as directed by a doctor.
  • Children under 6 years: as a doctor

OTHER SAFETY INFORMATION

  • Store in a cool and dry place

INACTIVE INGREDIENT SECTION

ascorbic acid (Vitamin C), aspartame, citric acid, extract of lemon balm and others extract herbs (elder, horehound, hyssop, lemon balm,linden flowers, mallow, peppermint, sage, thyme, wild thyme), isomalt, natural color (beta-carotene), natural flavors.

OTC - QUESTIONS SECTION

Questions? or to report and adverse event call: 1-833-552-1767

RECENT MAJOR CHANGES SECTION

  • Indications and Usage
  • Dosage and Administration
  • Contraindications
  • Warnings and Precautions
  • Inactive ingredients

Front Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFront

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
701201menthol 1.1 MG Oral LozengePSN1
701201menthol 1.1 MG Oral LozengeSCD1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0024-1Herbal Throat Drops45 in 1 BAGPASTILLE451

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-002479481-0024-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Herbal Throat DropsLEMON MINT HERBALMeijer, Inc.37dd58ad-95d1-568c-e063-6394a90a94332025-06-16WarningsExact identifier
ndc (package): 79481-0024-1
ndc (product): 79481-0024
ndc11 (package): 79481002401
spl id: 37dd5895-e629-6994-e063-6294a90a45e2
spl set id: 37dd58ad-95d1-568c-e063-6394a90a9433

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.