IODENT ANIMAL KINGDOM BUBBLE GUM- sodium fluoride paste

Iodent Animal Kingdom Bubble Gum by

Drug Labeling and Warnings

Iodent Animal Kingdom Bubble Gum 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 fluoride 0.22%---------------------------------------------------------------------------Anti-Cavity

(Available fluoride content:1000 ppm)

PURPOSE

Uses

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 the reach of children under 6 years of age.

INDICATIONS & USAGE

Direction:

Aduts 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.

Children under 6 years: Instruct children under 6 years of age to use a pea size amount. Supervise child's brushing and rinsing (to minimize swallowing).

Children under 2 years of age: Consult a dentist or physician.

INACTIVE INGREDIENT

Inactive ingredients

water, sorbitol, silica, polyethylene glycol 400, sodium carboxymethylcellulose, sodium lauryl alcohol, gum flavor, titanium dioxide, sodium saccharin, methylparaben, propylparaben, color: pink

DOSAGE & ADMINISTRATION

Distributed by:

United Exchange Corp.

17211 Valley View Ave.,

Cerritos, CA 90703 USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IODENT ANIMAL KINGDOM BUBBLE GUM 
sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-106
Route of Administration	DENTAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-106-85	1 in 1 CARTON
1		85 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	06/13/2014

Labeler - United Exchange Corp. (840130579)