OTC - ACTIVE INGREDIENT SECTION
Active ingredient 20 mg
Oral anesthetic
Severe Throat Drops
- Manufacturer
- Target Corporation Inc. | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
- Effective date
- 2024-07-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:14:43
Label at a glance#
ProductSevere Throat Drops
Active ingredientMENTHOL
Label structure14 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Uses temporarily relieves ocassional minor irritation and pain due toL
- Sore throat
- Sore mouth
INDICATIONS & USAGE SECTION
Uses 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 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
eucalytus oil, FD&C blue No.1, glucose syrup, gum arabic, sucrose
OTC - QUESTIONS SECTION
Questions? or to report and adverse event call: 1-800-910-68-74
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82442-201-01 | Severe Throat Drops | 45 in 1 BAG | PASTILLE | 45 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Severe Throat Drops
- Menthol Ice
- EUCALYPTOL
- FD&C BLUE NO. 1
- ACACIA
- SUCROSE
- CORN SYRUP
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82442-201 | 82442-201-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EUCALYPTOL | RV6J6604TK | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| ACACIA | 5C5403N26O | IACT |
| SUCROSE | C151H8M554 | IACT |
| CORN SYRUP | 9G5L16BK6N | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Severe Throat Drops | MENTHOL ICE | Target Corporation Inc. | 1876b221-fa60-5269-e063-6394a90a6963 | 2024-07-04 | Warnings | 82442-201-01 82442-201 82442020101 1c6cfa26-4422-62d9-e063-6394a90ad7b9 1876b221-fa60-5269-e063-6394a90a6963 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.