JASON SEA FRESH ANTICAVITY DEEP SEA SPEARMINT- sodium monofluorophosphate gel

Jason Sea Fresh Anticavity Deep Sea Spearmint by

Drug Labeling and Warnings

Jason Sea Fresh Anticavity Deep Sea Spearmint by is a Otc medication manufactured, distributed, or labeled by The Hain Celestial Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Monofluorophosphate 0.76%

PURPOSE

Anticavity

INDICATIONS & USAGE

use: Prevention of cavities

WARNINGS

Avoid storing at high temperatures (greater than 100°F). Protect from freezing. If you accidentally swalow more than used for brushing, seek professional assistance or contact Poison Control immediately.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children under 6 years of age.If you accidentally swallow more than used for brushing, get medical help or contact Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Prevent plaque and tartarbuildup with regular drushing. Adults and children 2 years of age or older should brush teeth after each meal (or at least twice a day, or as directed by a dentist or physician). Children under 6: Should use only a pea sized amount of paste and be supervised as necessary. Children under 2, check with a dentist or physician before using.

INACTIVE INGREDIENT

Glycerin, Aqua (Water), Hydrated Silica, Sodium Cocoyl Glutamate, Xylitol, Mentha Viridis (Spearmint) Leaf Oil, Aloe Barbadensis Leaf Juice (1), Bambusa Arundinacea Stem Powder, Carum Petroselinum (Parsley) Extract, Chlorella Pyrenoidosa Extract, Citrus Grandis (Grapefruit) Seed Extract, Perilla Ocymoides Seed Extract, Stevia Rebaudiana Leaf/Stem Extract, Ascorbic Acid, Tocopheryl Acetate, Calcium Carbonate, Cellulose Gum, Citric Acid, Sea Salt, Sodium Bicarbonate, Sodium Magnesium Silicate, Sodium Sulfate, Ubiquinone (2).

(1) Certified Organic Ingredients

(2) Coenzyme Q10

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

JASON SEA FRESH ANTICAVITY DEEP SEA SPEARMINT 
sodium monofluorophosphate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61995-0530
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.76 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CHLORELLA PYRENOIDOSA (UNII: 591BV50NV8)
SODIUM SULFATE (UNII: 0YPR65R21J)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5)
PARSLEY (UNII: 58FMD0Q0EV)
STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
SPEARMINT OIL (UNII: C3M81465G5)
UBIDECARENONE (UNII: EJ27X76M46)
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
SEA SALT (UNII: 87GE52P74G)
CALCIUM CARBONATE (UNII: H0G9379FGK)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61995-0530-6	1 in 1 CARTON	09/29/2017
1		170 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	09/29/2017

Labeler - The Hain Celestial Group, Inc. (117115556)

Registrant - The Hain Celestial Group, Inc. (014334364)

Establishment
Name	Address	ID/FEI	Business Operations
The Hain Celestial Group, Inc.		014334364	manufacture(61995-0530)