THERABREATH ANTICAVITY- sodium fluoride rinse 
Church & Dwight Co., Inc.

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Therabreath Anticavity Oral Rinse

Drug Facts

Active Ingredients

Sodium Fluoride 0.05% (0.02% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warnings

Keep out of the reach of children.If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and Children 18 years of age or older:

Other information

Do not use if safety seal is broken or missing

Inactive Ingredients

Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Citric Acid, Sodium Hydroxide, Sodium Chlorite, Menthol, Citrus Lemon Peel Oil, Mentha Piperita Oil, Sodium Benzoate, Sucralose, Xylitol, Sodium Bicarbonate.

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

FORMERLY
KNOWN AS
HEALTHY
SMILE

ANTICAVITY FLUORIDE RINSE

Thera Breath
DENTIST FORMULATED
ANTICAVITY
ORAL RINSE

HELPS FIGHT CAVITIES FOR 24 HOURS*
STRENGTHENS TEETH + ENAMEL • FRESHENS BREATH

Helps rebuild weakened tooth enamel and prevent tooth decay

No Alcohol • With Fluoride • Non Burning

IMPORTANT:
Read directions
for proper use.

16 fl.oz.
473 mL

SPARKLE MINT

Principal Display Panel - 473 mL Bottle Label
THERABREATH ANTICAVITY 
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-260
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.005 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
XYLITOL (UNII: VCQ006KQ1E)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-260-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/2023
2NDC:10237-260-011000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/202309/13/2026
3NDC:10237-260-0388.7 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/13/2023
Labeler - Church & Dwight Co., Inc. (001211952)

Revised: 11/2024
Document Id: 26587348-07ca-3c3a-e063-6394a90a383e
Set id: feab3d45-ff95-4b32-8258-7d932a7380c9
Version: 3
Effective Time: 20241107
 
Church & Dwight Co., Inc.