PROVETI DENTI PREMIUM

Manufacturer
SUN LIFE SCIENCE Co.,Ltd. | PL COSMETIC
Effective date
2022-03-08
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:41:21

Label at a glance#

ProductPROVETI DENTI PREMIUM
Active ingredientPOLIGLUSAM, PROPOLIS WAX
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Chitosan(Poliglusam), Propolis Wax(Extract)

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Mouthwash for pets and Get rid of bad breath.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUN LIFE LABELSUN LIFE LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86157-0001-1PROVETI DENTI PREMIUM50 mL in 1 BOTTLE, SPRAYLIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86157-0001PROVETI DENTI PREMIUM (POTASSIUM CARBONATE) LIQUID [SUN LIFE SCIENCE CO.,LTD.]11 package rows20220315_92d9d85a-3af3-4c09-a08c-817161e81ff5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86157-000186157-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLIGLUSAM82LKS4QV2YACTIM
PROPOLIS WAX6Y8XYV2NOFACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.