UNPA CHA CHA TOOTHPASTE JASMINE MINT- sodium monofluorophosphate paste, dentifrice 
Lycl Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

Sodium Monofluorophosphate 0.74%

INACTIVE INGREDIENTS

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

PURPOSE

Anti carries

WARNINGS

■ Contains 977ppm of fluoride.
■ Do not swallow and rinse mouth thoroughly after use
■ 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

■ Keeps breath fresh with a light fragrance
■ Helps protect against cavities
■ Helps to strengthen the teeth
■ Removal of plaque

Directions

■ Adults and children 2 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day or as directed by a dentist or doctor.
■ Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
■ Children under 2 years: Consult a dentist or doctor.

Other Information

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light (1~30℃)

QUESTIONS

■ unpaglobal.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

UNPA CHA CHA TOOTHPASTE JASMINE MINT 
sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73134-090
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.74 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Sorbitol (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73134-090-021 in 1 CARTON09/01/2021
1NDC:73134-090-01100 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35509/01/2021
Labeler - Lycl Inc. (689062275)
Registrant - Lycl Inc. (689062275)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(73134-090)

Revised: 9/2021
Document Id: 712eb317-5b51-42f2-a605-17e6e66d9351
Set id: a11ab5cf-a755-46a5-97d6-a80d92c8c969
Version: 1
Effective Time: 20210923
 
Lycl Inc.