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E ENZYME

Medically reviewed on November 14, 2017

Dosage form: paste, dentifrice
Ingredients: SODIUM MONOFLUOROPHOSPHATE 1.2g in 200g
Labeler: SAMJOKO SKYBLUE CO., LTD.
NDC Code: 76414-010

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.

Drug Facts

Active ingredient: SODIUM MONOFLUOROPHOSPHATE 0.6%

Inactive ingredients:

Water, D-Sorbitol Liquefied, Colloidal Silcon Dioxide, ATTAPULGITE, PEG-1500, Sluminum chlorohydroxg allautonate, Aminocaparoid Acid, Sodium Saccharine, XYLITOL, Butyl-P oxybenzoare, Hydroxyapatite, Carbon hydrozen Sodium, GLYCERIN, Carboxymethylcellulose nattrium, Sulfuricacid, GRAPEFRUIT SEED OIL, GREEN TEA LEAF, PROPOLIS WAX, I-mentol, Optimint

Purpose: Anticavity, remove plaque, bad breath, whiten tooth - it improved taste keeps mouth feeling fresh and clean.

Warnings:
It includes fluoride 792ppm
Children under 6 years of age: use a pea-size amount. Do not swallow. Supervis children's brushing until capable of using without supervision.
If children accidentally swallow more than used for brushing, ask a dentist or physician.

Keep out of reach of children:

Keep out of reach of children.

Indication and usage:
Aids in the prevention of cavities
Helps prevent gingivitis and alveolar pyorrhea

Dosage and administration:
Adults at least a half-inch strip of the product onto a soft bristled tooth brush.
Brush teeth thoroughly for at least 3 minutes twice a day.

E ENZYME 
sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76414-010
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (FLUORIDE ION) SODIUM MONOFLUOROPHOSPHATE1.2 g  in 200 g
Inactive Ingredients
Ingredient NameStrength
Water 
ATTAPULGITE 
XYLITOL 
GLYCERIN 
GRAPEFRUIT SEED OIL 
GREEN TEA LEAF 
PROPOLIS WAX 
Packaging
#Item CodePackage Description
1NDC:76414-010-01200 g in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35503/01/2011
Labeler - SAMJOKO SKYBLUE CO., LTD. (557804810)
Registrant - SAMJOKO SKYBLUE CO., LTD. (557804810)
Establishment
NameAddressID/FEIOperations
SAMJOKO SKYBLUE CO., LTD.557804810manufacture

 
SAMJOKO SKYBLUE CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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