Dosage and administration
■ adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed. ■ children under 5 years: ask a doctor.
■ adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed. ■ children under 5 years: ask a doctor.
■ 10 calories per drop ■ contains: SOY.
Menthol 5.4 mg
Purposes cough suppressant, oral anesthetic
temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat
Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or follow headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.
Ask a doctor before use if you have: ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema ■ cough accompanied by excessive phlegm (mucus).
Stop use and ask a doctor if ■ cough persists for more than 1 week, tends to recur, or is accompained by fever, rash, or persistent headache. These could be signs of a serius condition. ■ sore mouth does not improve in 7 days ■ irritation, pain, or redness persists or worsens.
Keep out of reach of children.
■ adults and children 5 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed.
■ children under 5 years: ask a doctor.
■ 10 calories per drop ■ contains: SOY.
Glucose syrup, sucralose, citric acid, eucalyptus oil, FD&C blue 1, FD&C red 40, flavors, potassium citrate, sucrose, soy lecithin, water
Or, to report an adverse event, call 800-245-2898.
Monday - Friday, 9 AM to APM EST
30 Drops NDC: 61658-885-30
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61658-885-30 | 2025-07-22 | C162847 | 48780-1 | 2cef2736-5e9e-d83d-e063-dadaa90ab31f | PV-MGC-YNBY Cough Drops Menthol 30 |
| 61658-885-30 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-5e9e-d83d-e063-dadaa90ab31f | PV-MGC-YNBY Cough Drops Menthol 30 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 61658-885 | 61658-885-30 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| POTASSIUM CITRATE | EE90ONI6FF | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| CORN SYRUP | 9G5L16BK6N | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| LECITHIN, SOYBEAN | 1DI56QDM62 | IACT |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| 3a8ea898-78de-85c9-e063-6294a90a9bcf | 01953d68-e52a-ea35-e063-6294a90a2f49 | 2025-07-22 | Warnings | 01953d68-e52a-ea35-e063-6294a90a2f49 |
Adverse event summaries are temporarily unavailable. Other product information remains available.