Breezers Creamy Strawberry

The listing

NDC product code

12546-352 (labeller 12546, product 352)

Labeller

Mondelez Global LLC

Brand name

Breezers Creamy Strawberry

Generic name

Pectin

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M022

Marketing start

3 August 2016

Listing expires

31 December 2026

RxNorm concept

700897

Active ingredients

Strengths as listed in the FDA National Drug Code Directory, retrieved 4 September 2026. "Other listings" counts every other product on this site containing the same ingredient at any strength.

What the label claims

These are read from this product's own label, not assigned by us and not inferred from the ingredient.

Stated purposeOral demulcent

Stated useSore throatSore mouth, gums and canker sores

Drug Facts, as filed

Quoted from the label FDA holds for this product. Long fields are truncated. The panel printed on the package you are holding is the one that governs.

Active ingredient

<(per drop) Pectin 7 mg>

Purpose

<Oral demulcent>

Uses

<temporarily relieves the following symptoms associated with sore mouth and sore throat: •minor discomfort • irritated areas>

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 may be serious.>

Stop use and ask a doctor if

<•sore mouth does not improve in 7 days • irritation, pain or redness persists or worsens>

Keep out of reach of children

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

<•adults and children 5 years and over: dissolve 1 or 2 drops (one at a time) slowly in the mouth. Repeat as needed. • children under 5 years: ask a doctor>

Inactive ingredients

<beta carotene, citric acid, FDC blue 2, FDC red 40, flavors, glucose syrup, lactic acid, malic acid, potassium citrate, sodium chloride, soy lecithin, sucrose, titanium dioxide, water>

Other information

<Call 1-800-524-2854, Monday to Friday, 9AM-5PM Eastern Time or visit our website at www.gethalls.com>

Label version 9, effective 20 December 2024. Retrieved from the openFDA drug label API on 4 September 2026. Read the full label on DailyMed.

Packages

The package NDC adds a third segment to the product code, identifying the pack size. See how to read an NDC.

Identical on the active ingredient

10 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 6 different labellers. They are not necessarily the same product: inactive ingredients, flavour and pack size differ, and this site does not compare prices.

Sources for this page

• FDA National Drug Code Directory entry for 12546-352
• DailyMed label, set id 777fd6db-f129-4489-8312-4b1aca94878e
• How Lozenges builds these pages