PROVETI DENTI PREMIUM- potassium carbonate liquid

PROVETI DENTI PREMIUM by

Drug Labeling and Warnings

PROVETI DENTI PREMIUM by is a Animal medication manufactured, distributed, or labeled by SUN LIFE SCIENCE Co.,Ltd., PL COSMETIC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Chitosan(Poliglusam), Propolis Wax(Extract)

INACTIVE INGREDIENT

water, ascorbic acid, stevioside, arginine, glycerin, tocopherol, dipropylene glycol, zantnoxylum piperitum fruit extract, pulsatilla koreana extract, usnea barbata (lichen) extract

PURPOSE

Mouthwash for pets and Get rid of bad breath.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Do not spray deep into the mouth, but spray on the molars and gums.

If it's hard to open your mouth, spray it around your mouth to encourage you to lick it.

Spray it to the mouth at least once or twice a day.

WARNINGS

A. Side effects
(1) Consult a veterinarian in case of any of the following abnormalities in use.If you have red spots, swelling, itching, or irritation during use.

B. Contraindications
Do not use it in areas with wounds.

C. Precautions for how to use it.
(1) If it goes into your eyes, wash it immediately.

D. Other precautions
(1) Store in a dry place after use.
(2) Store out of reach of infants and children.
(3) Do not store it in a hot or low temperature place or in a place where sunlight contacts.

DOSAGE & ADMINISTRATION

For external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROVETI DENTI PREMIUM 
potassium carbonate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 86157-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLIGLUSAM (UNII: 82LKS4QV2Y) (POLIGLUSAM - UNII:82LKS4QV2Y)	POLIGLUSAM	1 g  in 100 mL
PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF)	PROPOLIS WAX	0.1 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86157-0001-1	50 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/08/2022

Labeler - SUN LIFE SCIENCE Co.,Ltd. (695149648)

Establishment
Name	Address	ID/FEI	Business Operations
SUN LIFE SCIENCE Co.,Ltd.		695149648	api manufacture

Establishment
Name	Address	ID/FEI	Business Operations
PL COSMETIC		688393375	manufacture