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Olea Olidental

Medically reviewed on January 21, 2017

Dosage form: paste
Ingredients: SILICON DIOXIDE 170mg in 1g
Labeler: AJU PHARM CO., LTD.
NDC Code: 70417-002

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

Silicon Dioxide 17%

Dental Care

To improve dental health and bad breath

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 physician

Children 2 to 6 years use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)

Children under 2 years ask a dentist or physician

Keep out of the reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

Keep out of the reach of children under 6 years of age.

Aluminium Chlorohydroxy Allantoinate
Aminocaproic Acid
Chamomile Extract
Eucalyptus Extract
Sage Extract
Aloe Extract
Grapefruit Seed Extract
Propolis Powder
D-Sorbitol Solution
Concentrated Glycerin
Xantangum
Xylitol
Glucosyl Stevia
Olive Leaf Extract
Hydroxyapatite
Sodium Cocoyl Glutamate
Mint Flavor
Begamot Flavor
Solvent

OLEA OLIDENTAL 
silicon dioxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70417-002
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE170 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCLOXA 
AMINOCAPROIC ACID 
CHAMOMILE 
EUCALYPTUS GLOBULUS LEAF 
CLARY SAGE 
ALOE 
CITRUS PARADISI SEED 
PROPOLIS WAX 
GLYCERIN 
XANTHAN GUM 
XYLITOL 
GLUCOSYL STEVIOL 
OLEA EUROPAEA LEAF 
TRIBASIC CALCIUM PHOSPHATE 
SODIUM COCOYL GLUTAMATE 
Packaging
#Item CodePackage Description
1NDC:70417-002-021 TUBE in 1 CARTON
1NDC:70417-002-01120 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/17/2017
Labeler - AJU PHARM CO., LTD. (687982405)
Registrant - AJU PHARM CO., LTD. (687982405)
Establishment
NameAddressID/FEIOperations
AJU PHARM CO., LTD.687982405manufacture(70417-002)

 
AJU PHARM CO., LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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