Active Ingredients And Purpose
OTC - ACTIVE INGREDIENT SECTION
Active ingredient 5.8 mg Cough Suppressant Oral anesthetic
OTC - PURPOSE SECTION
Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat
Menthol Cough Drops
- Manufacturer
- Target Corporation Inc. | Boston Nutraceutical Science SL | Boston Nutraceutical Production SL
- Effective date
- 2025-01-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:53:43
Key Label Information#
Uses
INDICATIONS & USAGE SECTION
Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat
Warnings
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 - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
Directions And Dosage
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 Label Information
INACTIVE INGREDIENT SECTION
blackcurrant and black carrot extract (coloring), citric acid, flavors, glucose syrup, sucrose
OTC - QUESTIONS SECTION
Questions? or to report and adverse event call: 1-800-423-0139
Label Images#
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82442-001-01 | Menthol Cough Drops | 80 in 1 BAG | PASTILLE | 80 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
- Menthol Cough Drops
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82442-001 | 82442-001-01 |
Ingredients#
| Name | UNII | Kind |
|---|---|---|
| EUCALYPTOL | RV6J6604TK | IACT |
| BLACK CURRANT | 9755T40D11 | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| BLACK CARROT | 27793ZFD2L | IACT |
| CHERRY | BUC5I9595W | IACT |
| SUCROSE | C151H8M554 | IACT |
| CORN SYRUP | 9G5L16BK6N | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
Complete SPL Sections#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient 5.8 mg Cough Suppressant Oral anesthetic
OTC - PURPOSE SECTION
Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat
INDICATIONS & USAGE SECTION
Uses temporarily relieves: cough as may occur with a cold ocassional minor irritation and sore throat
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
blackcurrant and black carrot extract (coloring), citric acid, flavors, glucose syrup, sucrose
OTC - QUESTIONS SECTION
Questions? or to report and adverse event call: 1-800-423-0139