QFORET SHARON TOOTHPASTE by QGENETICS CO.,LTD. / K.Boeun Pharmaceutical Co.,Ltd.

QFORET SHARON TOOTHPASTE by

Drug Labeling and Warnings

QFORET SHARON TOOTHPASTE by is a Otc medication manufactured, distributed, or labeled by QGENETICS CO.,LTD., K.Boeun Pharmaceutical Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

QFORET SHARON TOOTHPASTE- sodium monofluorophosphate, silica, alcloxa paste, dentifrice 
QGENETICS CO.,LTD.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active ingredients

Sodium Monofluorophosphate 0.758%
Silica 15.00%
Alcloxa 0.11%

Inactive ingredients

Sorbitol,Glycerin,Cellulose Gum,Algin,Sodium Cocoyl Glutamate,Cocamidopropyl Betaine,Hydroxyapatite,Xylitol,Glucosyl Stevioside,Menthol,Mentha Piperita (Peppermint) Oil,Flavor,Pistacia Lentiscus (Mastic) Gum Oil,Myrrh Tincture,Citrus Grandis (Grapefruit) Seed Extract,Camellia Sinensis Leaf Extract,Chamomilla Recutita (Matricaria) Extract,Salvia Officinalis (Sage) Extract,Panax Ginseng Root Extract,Centella Asiatica Leaf Extract,Licorice Root Extract,Water

Purpose

ANTICAVITY
ANTI-PLAQUE
GUM CARE

Warnings

■ Keep out of reach of children under 6 years of age.
■ If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children

■ Keep out of reach of children under 6 years of age.

Uses

■ Aids in the prevention of dental cavities
■ Plaque removal (Anti-Plaque)
■ Prevention of periodontal disease, prevention of gum disease

Directions

■ Apply an appropriate amount to your toothbrush and brush your teeth by brushing.

Other Information

■ Store in an airtight container at room temperature
■ Date of use: 36 months from the date of manufacture

Question or Comments?

Email: qgenetics@qgenetics.co.kr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QFORET SHARON TOOTHPASTE 
sodium monofluorophosphate, silica, alcloxa paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83193-030
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.758 g  in 100 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	15 g  in 100 g
ALCLOXA (UNII: 18B8O9DQA2) (ALLANTOIN - UNII:344S277G0Z)	ALCLOXA	0.11 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83193-030-02	1 in 1 CARTON	05/01/2023	09/30/2024
1	NDC: 83193-030-01	120 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2023	09/30/2024

Labeler - QGENETICS CO.,LTD. (694619127)

Registrant - QGENETICS CO.,LTD. (694619127)

Establishment
Name	Address	ID/FEI	Business Operations
K.Boeun Pharmaceutical Co.,Ltd.		695674074	manufacture(83193-030)

Revised: 11/2025

Document Id: 4468896e-62d5-5fc0-e063-6294a90a053c

34390-5

Set id: 721ac434-f195-4062-80a1-db1c1be729b3

Version: 2

Effective Time: 20251125