PHYENLIMCIDE TOOTHPASTE- silicon dioxide paste, dentifrice

PHYENLIMCIDE TOOTHPASTE by

Drug Labeling and Warnings

PHYENLIMCIDE TOOTHPASTE by is a Otc medication manufactured, distributed, or labeled by WOORIZ Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Silicon Dioxide 15.0%

PURPOSE

Anticavity

Uses

■ Helps protect against cavities

WARNINGS

■ Do not swallow and rinse mouth thoroughly after use
■ For children under 6 years of age, use small amounts of toothpaste.
under the supervision of a guardian to avoid sucking or swallowing.
■ Consult a physician or dentist immediately if a child under 6 years old has
swallowed large quantities.
■ Keep out of the reach of children under 6 years of age.

KEEP OUT OF REACH OF CHILDREN

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

Directions

■ Adults and children 2 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day or as directed by a dentist or doctor.
■ Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
■ Children under 2 years: Consult a dentist or doctor.

Other Information

■Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

Questions

smartstore.naver.com/wooriz

INACTIVE INGREDIENTS

D-sorbitol Solution,L-Menthol,Sophora Extract,Glycerin,Aminocaproic Acid,Geen Tea Extract,Aluminum Chlorohydroxy Allantoinate,Lemon Extract,Mastic Oil,Myrrh Tincture,Sodium Saccharin,Aloe Extract(09),Eucalyptus Globulus Leaf Oil,Xylitol,Water,Sodium Chloride,Carboxymethylcellulose Sodium,Camomille Extract(1),Sodium Cocoyl Glutamate,Peppermint Oil,Chamaecyparis Obtusa Oil,Propolis Extract,Hydroxyapatite,Scutellaria Root Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHYENLIMCIDE TOOTHPASTE 
silicon dioxide paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82336-020
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Silicon Dioxide (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	Silicon Dioxide	15.0 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82336-020-02	1 in 1 CARTON	04/01/2022
1	NDC: 82336-020-01	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		04/01/2022

Labeler - WOORIZ Co.,Ltd. (695143249)

Registrant - WOORIZ Co.,Ltd. (695143249)

Establishment
Name	Address	ID/FEI	Business Operations
WOORIZ Co.,Ltd.		695143249	manufacture(82336-020)