FDA.reportPublic FDA data

Pectin Pops

Manufacturer
Walgreen Co. | BestCo Inc.
Effective date
2018-09-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:49:41

Label at a glance#

ProductPectin Pops
Active ingredientPECTIN
Label structure12 sections

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

  • 15 calories per pop
  • not a candy

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.

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

Walgreens Pectin Pops 20ctWalgreens Pectin Pops 20ct

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-1092-202022-07-05C16284748780-19d75b9cf-e048-f424-e053-dadaa90a57cePectin 10 mg
0363-1092-202020-01-31C16284748780-19d75b9cf-e048-f424-e053-dadaa90a57cePectin 10 mg

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
0363-10920363-1092-20

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
WATER059QF0KO0RIACT
PECTIN89NA02M4RXACTIB

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
e313fcab-6a9f-1aae-e053-2a95a90aec6153940d3b-45ff-00d1-e054-00144ff8d46c2022-07-05WarningsExact identifier
spl set id: 53940d3b-45ff-00d1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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