FINEFRA SILVER- sodium monofluorophosphate paste, dentifrice 
Jewoo Medical Co,.Ltd

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

Active ingredient: Sodium Monofluorophosphate 0.76%

INACTIVE INGREDIENT

Inactive ingredients: Silica, Dental type silica, 6-Aminocaproic Acid, Allantoine Chlorohydroxy Aluminum, Glycerin, Polyethylene Glycol 1500, D-Sorbitol Solution, Carboxymethylcellulose Sodium, Xylitol, Saccharin Sodium, Sodium Benzoate, Sodium Lauryl Sulfate, L-Menthol, Peppermint Oil, Carvone, Anethole, Silver, Mica, CI 42090, Purified Water

PURPOSE

Purpose : Anticavity

WARNINGS

Warnings: If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Indications & usage: help protect against gum disease and cavities.

DOSAGE & ADMINISTRATION

Dosage & administration: 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FINEFRA SILVER 
sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69653-020
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69653-020-01100 g in 1 CARTON; Type 0: Not a Combination Product03/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35503/01/2015
Labeler - Jewoo Medical Co,.Ltd (689512541)
Registrant - Jewoo Medical Co,.Ltd (689512541)
Establishment
NameAddressID/FEIBusiness Operations
NEO-MEDICALFARM CO.,LTD694914835manufacture(69653-020)

Revised: 11/2018
Document Id: 603cbaed-4cfb-4523-a6d7-c5292f7b86e4
Set id: 2ec1ce17-0528-4999-81be-3219f4623939
Version: 2
Effective Time: 20181129
 
Jewoo Medical Co,.Ltd