FLAVON WHITE MINT TOOTH- calcium carbonate, allantoin powder, dentifrice

FLAVON WHITE MINT TOOTH by

Drug Labeling and Warnings

FLAVON WHITE MINT TOOTH by is a Otc medication manufactured, distributed, or labeled by BS and Co. Ltd, BIOSTECH CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Calcium Carbonate 45.0%
Allantoin 1.0%

PURPOSE

Anti-plaque
Anti-gingivitis, Anti-Periodontitis

Uses

Aids in the removal of plaque and prevention gingivitis and periodontitis.

WARNINGS

Keep out of the reach of children under 6 years of age.
If you accidentally swallow more than used for brushing, seek professional help or contact a poison control center immediately.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Adults and children 2 yrs. older: Brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician. Do not swallow.
Children under 6 yrs.: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
Children under 2 yrs.: Ask a dentist or physician.

Other Information

Store at room temperature

QUESTIONS

Visit www.beauti-science.com/whitelabs/en

INACTIVE INGREDIENTS

Sorbitol, Sodium Bicarbonate, Sodium Lauryl Sulfate, Xylitol, Xanthan Gum, Mint Flavor, Menthol, Mentha Piperita Oil, Stevioside, Ascorbic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FLAVON WHITE MINT TOOTH 
calcium carbonate, allantoin powder, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73660-003
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Calcium Carbonate (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	45.0 g  in 100 g
Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	Allantoin	1.0 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Sorbitol (UNII: 506T60A25R)
Sodium Bicarbonate (UNII: 8MDF5V39QO)
Sodium Lauryl Sulfate (UNII: 368GB5141J)
Xylitol (UNII: VCQ006KQ1E)
Xanthan Gum (UNII: TTV12P4NEE)
Menthol (UNII: L7T10EIP3A)
PEPPERMINT OIL (UNII: AV092KU4JH)
Stevioside (UNII: 0YON5MXJ9P)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73660-003-02	1 in 1 CARTON	07/01/2020
1	NDC: 73660-003-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2020

Labeler - BS and Co. Ltd (689513606)

Registrant - BS and Co. Ltd (689513606)

Establishment
Name	Address	ID/FEI	Business Operations
BIOSTECH CO., LTD.		687294330	manufacture(73660-003)