DR. JEN SUPERPASTE NANO-HYDROXYAPATITE- sodium fluoride paste, dentifrice

Dr. Jen SuperPaste Nano-Hydroxyapatite by

Drug Labeling and Warnings

Dr. Jen SuperPaste Nano-Hydroxyapatite by is a Otc medication manufactured, distributed, or labeled by Dr Jen Natural, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS

Active Ingredient
Sodium Fluoride 0.22%

PURPOSE

Purpose:
Sodium Fluoride - Anticavity

INDICATIONS & USAGE

Use: Aids in the prevention of dental cavities

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
under 6 years of age.

DOSAGE & ADMINISTRATION

Directions: 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
doctor. Instruct children under 6
years of age in good brushing and
rinsing habits (to minimize
swallowing). Supervise children as
necessary until capable of using
without supervision. Children under
2 years of age: Consult a dentist or
doctor.

INACTIVE INGREDIENT

Inactive Ingredients: Water,
Glycerin, Hydrated Silica, Xylitol,
Nano-Hydroxyapatite, Calcium
Carbonate, Sodium Methyl Cocoyl
Taurate, Sodium Carboxymethyl-
cellulose, Natural Strawberry Flavor,
Stevia Rebaudiana Leaf Extract, Citric
Acid, Illicium Verum (Anise) Fruit
Extract, Carica Papaya Extract, Prunus
Serotina (Black Cherry) Bark Extract,
Glycyrrhiza Uralensis (Chinese Licorice)
Root Extract

Dr. Jen SuperPaste Product Package Labeling

Dr. Jen

Super Paste

TRIPLE CAVITY
PROTECTION

10% NANO-HYDROXYAPATITE,
FLUORIDE & XYLITOL
TOOTHPASTE

Strawberry

3.4 FL. OZ. | 100 ML

DrJenNatural.com

Dr. Jen
St. Paul, MN 55118

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INGREDIENTS AND APPEARANCE

DR. JEN SUPERPASTE NANO-HYDROXYAPATITE 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84181-735
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.22 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
XYLITOL (UNII: VCQ006KQ1E)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
CALCIUM CARBONATE (UNII: H0G9379FGK)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
STAR ANISE FRUIT (UNII: CK15HA8438)
CARICA PAPAYA LEAF (UNII: 66J7636Z2I)
PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	STRAWBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84181-735-07	1 in 1 BOX	03/21/2024
1		100 mL 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 Drug	M021	03/21/2024

Labeler - Dr Jen Natural, LLC (042902683)

Registrant - Dr Jen Natural, LLC (042902683)