IDODENT FLOURIDE MINT- fluoride paste

Idodent Flouride Mint by

Drug Labeling and Warnings

Idodent Flouride Mint by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                                                                 Purpose

Sodium monofluorophosphate 0.76%---------------------------------------------------- Anticavity

(Total Fluoride Content - 1000 ppm Approx.)

PURPOSE

Uses

Regular brushing with fluoride toothpaste helps protect teeth and roots against cavities

WARNINGS

Warnings

KEEP OUT OF REACH OF CHILDREN

Warnings

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

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Directions

• Adults and children 2 years and older: Brush Teeth thoroughly after meals, twice a day, or use as directed by a dentist or physician.
• Children under 6 years: To minimize swallowing use a pea-sized amount and supervise brushing until good habits are established.
• Children under 2 years: Ask a dentist or physician.

STORAGE AND HANDLING

Other Information

Store at room temperature 20-25°C (68-77°F)

INACTIVE INGREDIENT

Inactive ingredients

calcium carbonate, water, sorbitol, hydrated silica, sodium lauryl sulfate, flavor, cellulose gum, sodium silicate, tetrasodium, propphosphate, sodium saccharin, titanium dioxide, methylparaben, PEG-8, propylparaben

DOSAGE & ADMINISTRATION

Distributed by:

United Exchange Corp.

17211 Valley View Ave.

Cerritos, CA 90703 USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IDODENT FLOURIDE MINT 
fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-181
Route of Administration	DENTAL

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
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
CALCIUM CARBONATE (UNII: H0G9379FGK)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
SORBITOL (UNII: 506T60A25R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM SILICATE (UNII: IJF18F77L3)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-181-18	1 in 1 CARTON	12/21/2016
1		181 g in 1 TUBE; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	10/23/2014

Labeler - United Exchange Corp. (840130579)