E ENZYME- sodium monofluorophosphate paste, dentifrice

E ENZYME by

Drug Labeling and Warnings

E ENZYME by is a Otc medication manufactured, distributed, or labeled by SAMJOKO SKYBLUE CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: SODIUM MONOFLUOROPHOSPHATE 0.6%

INACTIVE INGREDIENT

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

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

WARNINGS

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:

Keep out of reach of children.

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

E ENZYME 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76414-010
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM MONOFLUOROPHOSPHATE	1.2 g  in 200 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ATTAPULGITE (UNII: U6V729APAM)
XYLITOL (UNII: VCQ006KQ1E)
GLYCERIN (UNII: PDC6A3C0OX)
GRAPEFRUIT SEED OIL (UNII: 598D944HOL)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76414-010-01	200 g in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	03/01/2011

Labeler - SAMJOKO SKYBLUE CO., LTD. (557804810)

Registrant - SAMJOKO SKYBLUE CO., LTD. (557804810)

Establishment
Name	Address	ID/FEI	Business Operations
SAMJOKO SKYBLUE CO., LTD.		557804810	manufacture