Sundown Honey Soothers Lollipops

Manufacturer
The Nature's Bounty Company
Effective date
2018-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:49

Label at a glance#

ProductSundown Honey Soothers Lollipops
Active ingredientPECTIN
Label structure12 sections

Indications and uses

For the temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat.

Dosage and administration

■ Adults and children 4 years of age and older: Allow product to dissolve slowly in mouth. May be repeated as needed or as directed by a doctor. ■ Children under 4 years of age: Consult a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

In each Lollipop:

Pectin 5.4 mg..............................................................Oral demulcent

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat.

Uses

OTC - PURPOSE SECTION

For the temporary relief of minor discomfort and protection of
irritated areas in sore mouth and sore throat.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 4 years of age and older: Allow product to
dissolve slowly in mouth. May be repeated as needed or as directed
by a doctor.
■ Children under 4 years of age: Consult a doctor.

Sore throat warning:

WARNINGS SECTION

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 may be serious.
Discontinue use and consult a doctor if:
■ sore mouth does not improve in 7 days
■ irritation, pain or redness persists or worsens
Keep out of reach of children

Sore throat warning:

OTC - ASK DOCTOR SECTION

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 may be serious.

Discontinue use and consult a doctor if:

OTC - STOP USE SECTION

■ sore mouth does not improve in 7 days
■ irritation, pain or redness persists or worsens

Directions

INSTRUCTIONS FOR USE SECTION

■ Adults and children 4 years of age and older: Allow product to
dissolve slowly in mouth. May be repeated as needed or as directed
by a doctor.
■ Children under 4 years of age: Consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citric acid, evaporated cane sugar, natural flavor, organic honey,
organic rice syrup, sodium citrate, sucrose, water

Questions?

OTC - QUESTIONS SECTION

Call 1-888-VITAHELP (848-2435)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Orange flavorOrange flavor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Raspberry flavorRaspberry flavor

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24737-1902-22021-01-29C16284748780-1ba0f9c33-58f8-a910-e053-dadaa90a0b857e18b870-24e7-eeea-e053-2a91aa0a909c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24737-1902-2Sundown Honey Soothers Lollipops60 g in 1 CARTONLOZENGE601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24737-1902SUNDOWN HONEY SOOTHERS LOLLIPOPS (PECTIN) LOZENGE [THE NATURE'S BOUNTY COMPANY]1Legacy NDC, 1 package rows20190701_7e18b870-24e7-eeea-e053-2a91aa0a909c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24737-190224737-1902-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PECTIN89NA02M4RXACTIB
SUCROSEC151H8M554IACT
WATER059QF0KO0RIACT
HONEYY9H1V576FHIACT

Source Document#

Source XML · Source PDF

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
7e18b870-24e8-eeea-e053-2a91aa0a909c7e18b870-24e7-eeea-e053-2a91aa0a909c2018-12-28WarningsExact identifier
spl id: 7e18b870-24e8-eeea-e053-2a91aa0a909c
spl set id: 7e18b870-24e7-eeea-e053-2a91aa0a909c

Reported adverse events (FAERS/openFDA)#

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