SMART BRUSHING TOOTH- allantoin paste, dentifrice

Smart Brushing Tooth by

Drug Labeling and Warnings

Smart Brushing Tooth by is a Otc medication manufactured, distributed, or labeled by Guardian Angel Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ALLATOIN

PURPOSE

For dental care

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Open one of these products and brush your teeth by brushing your teeth.

WARNINGS

Storage method

1. Keep it at room temperature in a classified container.

2. Cover and store at room temperature.

3. Store in a not moisture and cool place.

4. Air may come out during use of this product, but there is no problem with its weight.

Usage Precautions

1. Be careful not to swallow. Rinse mouth thoroughly after use

2. If the use of toothpaste causes abnormalities such as gums or mouth injury, discontinue use and consult a doctor or dentist.

3. For children under 6 years of age, use a small amount of toothpaste as small as pea per use, and use under the guidance of a guardian to avoid sucking or swallowing.

4. If a child under 6 years old swallows large amount, consult with a doctor or dentist immediately.

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

INACTIVE INGREDIENT

GLYCERIN

XYLITOL

STEVIOL GLYCOSIDE

ERYTHRITOL

CITRIC ACID

SODIUM CITRATE

BLUE NO1 (BRILLIANT BLUE) 1/250

ASCORBIC ACID

SODIUM LAURYL SULFATE

METHYL P-HYDROXYBENZOATE

CARBOXYMETHYL CELLULOSE

POE(60) HYDROGENATED CASTOR OIL

PEPPERMINT

EUCALYPTUS OIL

LEMON OIL

L-MENTHOL

ETHANOL

WATER

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SMART BRUSHING TOOTH 
allantoin paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69086-0001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.1 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69086-0001-1	24 in 1 BOX	05/01/2019
1		0.2 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2019

Labeler - Guardian Angel Co.,Ltd. (688150332)

Registrant - Guardian Angel Co.,Ltd. (688150332)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Angel Co.,Ltd.		688150332	manufacture(69086-0001) , label(69086-0001)