Throat relief pops
- Manufacturer
- CVS Pharmacy | Bestco Inc.
- Effective date
- 2023-10-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:23:40
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each pop)
Pectin 10 mg
OTC - PURPOSE SECTION
Purpose
Oral demulcent
INDICATIONS & USAGE SECTION
Uses
For temporary relief of minor discomfort and protection of irritated areas in sore mouth 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, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.
OTC - STOP USE SECTION
Stop use and ask doctor if
irritation, pain or redness persists 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 3 years and over - allow 1 pop to dissolve slowly in mouth. May be repeated as necessary or as directed by a doctor.
children under 3 years - ask a doctor
OTHER SAFETY INFORMATION
Other information:
Not a candy
INACTIVE INGREDIENT SECTION
Inactive ingredients: Ascorbic acid, citric acid, corn starch, corn syrup, FD&C blue no. 1, FD&C red no. 40, glycerin, medium chain triglycerides, natural and artificial flavors, sodium ascorbate, soybean oil, sucrose, water, and zinc gluconate.
OTC - QUESTIONS SECTION
Questions? Or to report an adverse event call 1-800-245-2898. Monday through Friday, 9AM to 4PM EST
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Throat relief pops
- pectin
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69842-364 | 69842-364-20 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PECTIN | 89NA02M4RX | 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 |
|---|---|---|---|---|---|---|
| 08289e08-9f15-21cc-e063-6294a90aada2 | 4ab4c460-f43e-0b29-e054-00144ff8d46c | 2023-10-20 | Warnings | 08289e08-9f15-21cc-e063-6294a90aada2 4ab4c460-f43e-0b29-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
