UNPA CHA CHA TOOTHPASTE- sodium monofluorophosphate paste, dentifrice

unpa Cha Cha Toothpaste by

Drug Labeling and Warnings

unpa Cha Cha 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

Sorbitol, Water, Silica, Glycerin, Sodium Cocoyl Glutamate, Cellulose Gum, Menthol, Mint Flavor, Carbon, Mentha Piperita (Peppermint) Oil, Xylitol, Mentha Viridis (Spearmint) Leaf Oil, Stevioside, Glycyrrhiza Glabra (Licorice) Root Extract, Taraxacum Officinale (Dandelion) Rhizome, Salvia Officinalis (Sage) Leaf Extract

PURPOSE

Caries prevention

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

(+82)1661 - 5981
www.unpacosmetics.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UNPA CHA CHA TOOTHPASTE 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73134-040
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
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73134-040-02	1 in 1 CARTON	02/01/2021
1	NDC: 73134-040-01	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	02/01/2021

Labeler - Lycl Inc. (689062275)

Registrant - Lycl Inc. (689062275)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(73134-040)