Throat Relief Pops

Manufacturer
Meijer Corporation | Bestco Inc.
Effective date
2023-10-26
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:23:11

Label at a glance#

ProductThroat Relief Pops
Active ingredientPECTIN
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each pop)

Pectin 10mg

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

INACTIVE INGREDIENT SECTION

Inactive ingredients: Ascorbic acid, citric acid, corn starch, corn syrup, FD&C Blue #1, FD&C Red #40, glycerin, medium chain triglycerides, natural and artificial flavors, sodium ascorbate, soybean oil, sucrose, water and zinc gluconate.

OTHER SAFETY INFORMATION

Other information:

Not a candy

OTC - QUESTIONS SECTION

Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Meijer Throat Pop 20ctMeijer Throat Pop 20ct

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-14541250-145-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
PECTIN89NA02M4RXACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
08a329e2-c8ed-8ffa-e063-6394a90a69cd4d76da2b-c81d-2cea-e054-00144ff8d46c2023-10-26WarningsExact identifier
spl id: 08a329e2-c8ed-8ffa-e063-6394a90a69cd
spl set id: 4d76da2b-c81d-2cea-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.