Unpa Cha Cha Premium Whitening Tooth by Lycl Inc. / DONG IL PHARMS CO., LTD.

Unpa Cha Cha Premium Whitening Tooth by

Drug Labeling and Warnings

Unpa Cha Cha Premium Whitening Tooth by is a Otc medication manufactured, distributed, or labeled by Lycl Inc., DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UNPA CHA CHA PREMIUM WHITENING TOOTH- hydrogen peroxide, silicon dioxide paste, dentifrice 
Lycl Inc.

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 INGREDIENT

Active Ingredient: Hydrogen Peroxide 2.14%, Silicon Dioxide 7.00%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, PEG-32, Sodium Cocoyl Glutamate, Xantan gum, Xylitol, Menthol, Flavor, Stevioside, Camellia Sinensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Eucalyptus Globulus Leaf Extract, Salvia Officinalis (Sage) Extract, Aloe Barbadensis Leaf Extract, Hydroxyapatite, Disodium EDTA

PURPOSE

Purpose: Whitening, Anti plaque

WARNINGS

Warnings:

1. Do not use for any other purposes except brushing your teeth.
2. Do not swallow, and rinse your mouth adequately after use.
3. Consult your physician or dentist and follow their directions if you swallow a large amount of toothpaste.
4. Discontinue use and consult your physician or dentist if gum or mouth pain occurs after using this toothpaste
5. Keep out of reach of children and guide them if they use this toothpaste.
6. Store it away from high or low temperature and from direct sunlight.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and guide them if they use this toothpaste.

Uses

Uses:
■ Promotes dental health and removes bad breath, makes teeth bright

Directions

Directions
■ Brush the teeth with a suitable amount.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UNPA CHA CHA PREMIUM WHITENING TOOTH 
hydrogen peroxide, silicon dioxide paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73134-030
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6.30 g  in 90 g
Hydrogen Peroxide (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	Hydrogen Peroxide	1.92 g  in 90 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73134-030-02	1 in 1 CARTON	11/01/2019	12/22/2019
1	NDC: 73134-030-01	90 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		11/01/2019	12/22/2019

Labeler - Lycl Inc. (689062275)

Registrant - Lycl Inc. (689062275)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(73134-030)

Revised: 12/2019

Document Id: 1725779a-494c-457d-b7cf-088003533d5e

34390-5

Set id: 3ce27ceb-4378-45da-8c5c-156a9304d1df

Version: 2

Effective Time: 20191224