SF menthol cough drop
- Manufacturer
- United Natural Foods, Inc. dba UNFI | Bestco, Inc
- Effective date
- 2024-01-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:14:08
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each drop)
Menthol 5.8mg
OTC - PURPOSE SECTION
Purposes
Cough suppressant / Oral anesthetic
INDICATIONS & USAGE SECTION
Uses temporarily relieves:
- cough as may occur with a cold
- occasional minor irritation and 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, headaches, 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
Ask a doctor before use if you have:
- persistent or chronic cough such as occurs with smoking, asthma, or emphysema
- cough accompanied by excessive phegm (mucus)
OTC - STOP USE SECTION
Stop use and consult doctor if
- cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
- sore throat is severe, or irritation, pain or redness lasts 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 reach of children.
DOSAGE & ADMINISTRATION SECTION
Directions
Adults and children 5 years and over - dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.
Children under 5 years - ask a doctor
OTHER SAFETY INFORMATION
Other information
- 6 calories per drop
- Excess consumption may cause a laxative effect.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Acesulfame potassium, corn starch, eucalyptus oil, FD&C blue no 1, FD&C red no. 40, glycerin, gum arabic, isomalt, maltitol syrup, medium chain triglycerides, natural and artificial flavors, potassium sorbate, soybean oil, sucralose and water.
OTC - QUESTIONS SECTION
Questions? Or to report an adverse event call 1-877-932-7948.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- SF menthol cough drop
- menthol
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 41163-027 | 41163-027-25 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| 46696ad8-c351-421f-e063-6294a90aff9b | 46c466d7-26ca-5179-e054-00144ff88e88 | 2025-12-20 | Warnings | 46c466d7-26ca-5179-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
