THERABREATH PLUS FRESH BREATH- sodium fluoride paste, dentifrice 
Church & Dwight Co., Inc.

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TheraBreath® Plus Fresh Breath

Drug Facts

Active Ingredients

Sodium fluoride 0.24% (0.14% W/V fluoride ion)

Purpose

Anticavity Fluoride Dentifrice

Uses

Aids in the prevention of dental cavities

Warnings

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults & 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.

Other information

Inactive Ingredients

Sorbitol, Water (Aqua), Hydrated Silica, Glycerin (from vegetable sources), Xylitol, Natural Flavor, Cellulose Gum, Tetrapotassium Pyrophosphate, Tetrasodium Pyrophosphate, Sodium Benzoate, Aloe Barbadensis Leaf Juice, Citric Acid, Sodium Chlorite, Zinc Gluconate, Ammonium Glycyrrhizate, Ascorbic Acid (Vitamin C), Ubiquinone (COQ10), Mentha Arvensis (Cornmint) Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Natural Fragrance (Parfum)

PRINCIPAL DISPLAY PANEL - 113.5 g Tube Label

ANTICAVITY TOOTHPASTE

CLINICAL FORMULA
TheraBreath®
PLUS

MAXIMUM STRENGTH

FRESH BREATH

TOOTHPASTE

FRESHENS BREATH FOR 24 HOURS*

Fortified with Zinc, Xylitol and Aloe
Nothing Works Faster and Lasts Longer
to Prevent Bad Breath

Dr. Harold Katz

net wt. 4 oz. • 113.5 g

PEPPERMINT

Principal Display Panel - 113.5 g Tube Label
THERABREATH PLUS FRESH BREATH 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-264
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.24 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
GLYCERIN (UNII: PDC6A3C0OX)  
XYLITOL (UNII: VCQ006KQ1E)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
POTASSIUM PYROPHOSPHATE (UNII: B9W4019H5G)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
UBIDECARENONE (UNII: EJ27X76M46)  
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  
SPEARMINT OIL (UNII: C3M81465G5)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-264-04113.5 g in 1 TUBE; Type 0: Not a Combination Product02/28/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH DRUGM02101/01/2024
Labeler - Church & Dwight Co., Inc. (001211952)

Revised: 1/2024
Document Id: a9edac39-2cc7-41be-9058-e8e490b18d26
Set id: a4dba786-df60-4b4f-85d9-636e275664af
Version: 1
Effective Time: 20240101
 
Church & Dwight Co., Inc.