UNPA CHA CHA ENERGY TOOTHPASTE- sodium monofluorophosphate paste, dentifrice

unpa Cha Cha Energy Toothpaste by

Drug Labeling and Warnings

unpa Cha Cha Energy Toothpaste 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]

ACTIVE INGREDIENT

Sodium Monofluorophosphate 0.74%

INACTIVE INGREDIENTS

Silicon Dioxide, Allantoin Chlorohydroxy Aluminum, Sodium Carboxymethyl Cellulose, D-Sorbitol Liquid, Concentrated Glycerin, Licorice Extract, Mastic Oil, Sage Extract, Matricaria Extract, Aloe Extract (09), Enzymatically Modified Stevia, Xylitol, L-menthol, Activated Charcoal, Mint Scent, Spearmint Oil, Anethole, Sodium Bicarbonate, Hydroxyapatite, Titanium Dioxide, Sodium Cocoyl Glutamate, Purified Water

PURPOSE

Gum Care

WARNINGS

■ Contains 977ppm of fluoride.
■ Do not swallow and rinse mouth thoroughly after use
■ If you experience any problems with your gums or mouth during use, discontinue use and consult your doctor.
■ For children under 6 years of age, use small amounts of toothpaste. And use it 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.

Uses

■ Keep your teeth white and strong.
■ Keep your mouth clean.
■ Refresh the inside of the mouth.
■ Prevents tooth decay caused by fluoride and removes bad breath.
■ Increases aesthetic effect.
■ Prevention of plaque deposition, removal of plaque (anti-prag)

Directions

Brushing the teeth with a suitable amount

Other Information

■ Airtight container, Store in normal temperature (1~30℃)

QUESTIONS

■ unpaglobal.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UNPA CHA CHA ENERGY TOOTHPASTE 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73134-070
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.74 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Silicon Dioxide (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73134-070-02	1 in 1 CARTON	05/01/2021
1	NDC: 73134-070-01	100 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
OTC monograph final	part355	05/01/2021

Labeler - Lycl Inc. (689062275)

Registrant - Lycl Inc. (689062275)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(73134-070)