FRAICHE 5000 KIDS PLUS DENTAL BUBBLE GUM- sodium fluoride,tribasic calcium phosphate gel

FRAICHE 5000 KIDS PLUS DENTAL BUBBLE GUM by

Drug Labeling and Warnings

FRAICHE 5000 KIDS PLUS DENTAL BUBBLE GUM by is a Prescription medication manufactured, distributed, or labeled by True Marker Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (s)                                                                       Purpose

1.1% neutral sodium fluoride and 4% calcium hydroxyapatite            Dental gel  

PURPOSE

Uses

This 1.1% neutral sodium fluoride and 4% calcium hydroxyapatite dental gel is intended to aid in the prevention of dental decay and to help treat tooth sensitivity to cold, heat, sweets, acids, or contact.

Directions

Use twice a day (morning and evening) in place of regular toothpaste or as recommended by a dentist or a physician. Adults and children 6 years of age and older. Twist off cap and remove foil seal. Apply at least a 1-inch strip of gel onto a soft bristle toothbrush. Brush teeth thoroughly for
at least 1 minute. Spit out and rinse mouth thoroughly. Make sure to brush all sensitive areas of the teeth.

KEEP OUT OF REACH OF CHILDREN

Children under 6 Years of Age: Consult a dentist or physician.

Dosage Form and Strengths

Dental gel containing 1.1% sodium fluoride and 4% calcium hydroxyapatite.

Contraindications

Avoid use in patients with known hypersensitivity to fluoride. Do not use in pediatric patients under 6 unless directed by a dentist or physician.

Warnings and Precautions

Do not swallow. Keep out of reach of children. Read the prescribing information fully before using this product. If the product is accidentally swallowed in quantities greater than would normally occur with a toothpaste, seek medical help right away. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4
weeks unless recommended by a dentist or physician.

Adverse Reactions

To report suspected adverse reactions, contact True Marker Pharmaceuticals at (877) 887-9879 or the FDA at (800) FDA-1088 or www.fda.gov/medwatch.

Description

Fraiche 5000 Kids Plus dental gel is a flavored, pH neutral 1.1% sodium fluoride and 4% calcium hydroxyapatite that aids in the prevention of dental decay and helps to treat sensitive teeth.

Inactive Ingredients

Water, Glycerin, Hydrated Silica, Calcium Carbonate, Xylitol, Sorbitol, Xanthan Gum, Flavor, Yucca Shidigera Root Extract, Quillaja Saponaria Bark Extract, Smilax Aristolochiaefolia Root Extract, Dioscorea Villosa Root Extract,Tocopheryl Acetate, Cocamidopropyl Betaine, Benzyl Alcohol.

How Supplied/Storage

4.3 ounces (122g) in plastic tube. Store at room temperature 59-86°F (15-30°C)

Product label

INGREDIENTS AND APPEARANCE

FRAICHE 5000 KIDS PLUS DENTAL BUBBLE GUM 
sodium fluoride,tribasic calcium phosphate gel

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 83592-818
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.1 g  in 100 g
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
CALCIUM CARBONATE (UNII: H0G9379FGK)
XYLITOL (UNII: VCQ006KQ1E)
SORBITOL (UNII: 506T60A25R)
XANTHAN GUM (UNII: TTV12P4NEE)
YUCCA SCHIDIGERA WHOLE (UNII: 08A0YG3VIC)
QUILLAJA SAPONARIA BARK (UNII: 8N0K3807ZW)
SMILAX ARISTOLOCHIIFOLIA ROOT (UNII: NR100Y25G0)
DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83592-818-04	1 in 1 CARTON	08/26/2024
1		40 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
unapproved drug other		08/26/2024

Labeler - True Marker Pharmaceuticals, Inc. (119046582)