Multi effect mouthwash

Manufacturer
NICEDAE GROUP LLC
Effective date
2025-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:36:27

Label at a glance#

ProductMulti effect mouthwash
Active ingredientCETYLPYRIDINIUM CHLORIDE, SODIUM FLUORIDE
Label structure12 sections

Dosage and administration

Open the packet along the dotted line, rinse your mouth for 30 seconds and spitit out. Do not swallow.

Storage and handling

This product contains plant extracts. If there is a small amount of precipitation. It is a normal phenomenon and can be used with confidence.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.05%

Cetylpyridinium Chloride 0.02%

Purpose

OTC - PURPOSE SECTION

Anticavity
Antiseptic

Use

INDICATIONS & USAGE SECTION

Use: Aids in the prevention of dental cavities and reduces oral bacteria.

Warnings

WARNINGS SECTION

●Do not use ifyou are allergic to any ingredient in this product or in children under 12 without dental advice.
●When using this product, do not swallow, avoid contact with eyes. If contact occurs, rinse thoroughly with water.
●Stop use and ask a doctor if irnitation, swelling, or rash develops.
●Keep out of reach of children. If swallowed, immediately seek medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

Do not use ifyou are allergic to any ingredient in this product or in children under 12 without dental advice.

OTC - WHEN USING SECTION

When using this product, do not swallow, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if iritation, swelling, or rash develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, immediately seek medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Open the packet along the dotted line, rinse your mouth for 30 seconds and spitit out. Do not swallow.

Other information

STORAGE AND HANDLING SECTION

This product contains plant extracts. If there is a small amount of precipitation. It is a normal phenomenon and can be used with confidence.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, SORBITOL ERYTHRITOL, PROPYLENE GLYCOL, XYLUTOL, POTASSIUM SORBATE, POLYSORBATE 20, SODIUM BENZOATE, AROMA DIPOTASSIUM GLYCYRRHIZATE, CITRIC ACID, DISODIUM EDTA, PANAX GINSENG EXTRACT, COPTIS CHINENSIS ROOT EXTRACT, PHELLODENDRON AMURENSE BARK EXTRACT, CURCUMALONGA (TURMERIC) ROOT EXTRACT,ANGELICAPOLYMORPHA SINENSIS ROOT EXTRACT, REHMANNIA GLUTINOSAROOT EXTRACT, SODIUMCITRATE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85824-00285824-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
48c91d95-50b0-7f26-e063-6394a90af4b938754b69-3c75-b139-e063-6394a90a8bb92026-01-19WarningsExact identifier
spl set id: 38754b69-3c75-b139-e063-6394a90a8bb9

Reported adverse events (FAERS/openFDA)#

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