FDA.reportPublic FDA data

Severe Throat Sore Drops

Manufacturer
Target Corporation Inc. | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
Effective date
2024-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:23:05

Label at a glance#

ProductSevere Throat Sore Drops
Active ingredientMENTHOL
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient in each drop Purposes

Menthol 20mg Cough Suppressant

Oral anesthetic

OTC - PURPOSE SECTION

Temporarily relieves ocassional minor irritation and pain due to:

  • sore throat
  • sore mouth

INDICATIONS & USAGE SECTION

Temporarily relieves ocassional minor irritation and pain due to:

  • sore throat
  • sore mouth

WARNINGS SECTION

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.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • a severe throat accompanied by difficulty in breathing or that last more than 2 days
  • a sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting

OTC - STOP USE SECTION

Stop use and consult a doctor if

  • sore mouth symptons do not improve in 7 days or if irritation, pains or redness persists or worsens.

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 this and all drugs out of the reach of children.

OVERDOSAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 12 years and over: dissolve 1 drop slowly in mouth. Repeated every 2 hours as needed or as directed by a doctor.
  • Children under 12 years and under do not use

OTHER SAFETY INFORMATION

  • Store in a cool and dry place

INACTIVE INGREDIENT SECTION

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

Back LabelBack Label

OTC - QUESTIONS SECTION

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

Monday to Friday 9AM to 4 PM east

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-143-012023-01-10C16284748780-1ba0f9c33-47b2-a910-e053-dadaa90a0b85Severe Throat Drops Oral Anesthetic
11673-143-012021-01-29C16284748780-1ba0f9c33-47b2-a910-e053-dadaa90a0b85Severe Throat Drops Oral Anesthetic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-143-01Severe Throat Sore Drops45 in 1 BAGPASTILLE453

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-143SEVERE THROAT SORE DROPS (MENTHOL) PASTILLE [TARGET CORPORATION INC.]3Current NDC, Legacy NDC, 1 package rows20241009_949543d5-5043-ac06-e053-2995a90ab398.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-14311673-143-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS OIL2R04ONI662IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
WATER059QF0KO0RIACT
ACACIA5C5403N26OIACT
SUCROSEC151H8M554IACT
CORN SYRUP9G5L16BK6NIACT
MENTHOLL7T10EIP3AACTIB

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
Severe Throat Sore DropsMENTHOLTarget Corporation Inc.949543d5-5043-ac06-e053-2995a90ab3982024-10-07WarningsExact identifier
ndc (package): 11673-143-01
ndc (product): 11673-143
ndc11 (package): 11673014301
spl id: 23e54a26-5a82-2024-e063-6294a90a2aa3
spl set id: 949543d5-5043-ac06-e053-2995a90ab398

Reported adverse events (FAERS/openFDA)#

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