THERABREATH OVERNIGHT CHAMOMILE MINT- sodium fluoride rinse 
Church & Dwight Co., Inc.

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Therabreath Overnight Chamomile Mint

Drug Facts

Active Ingredients

Sodium Fluoride 0.05% (0.02% wh 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, gel medical help or contact a Poison Control Center right away.

Do not use with another fluoride rinse on the same day.

Directions

Adults 18 years of age or older:

Other information

Do not use if safety seal is broken or missing

Inactive Ingredients

Water, Flavor, Citric Acid, Glycerin, Menthol, PEG-40 Hydrogenated Castor Oil, Sodium Benzoate, Sodium Bicarbonate, Sodium Chlorite, Sodium Hydroxide, Sucralose

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

ANTICAVITY FLUORIDE RINSE

STRENGTHENS
TEETH

TheraBreath
DENTIST FORMULATED
OVERNIGHT
ORAL RINSE

FIGHTS BAD BREATH FOR 12 HOURS*
HELPS PREVENT CAVITIES & REBUILD ENAMEL

No Alcohol • No Dyes
Non Burning

IMPORTANT:
Read directions
for proper use.

16 fl. oz.
473 mL

CHAMOMILE MINT

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
THERABREATH OVERNIGHT CHAMOMILE MINT 
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-262
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION5 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)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMENTHOL, MINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-262-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/22/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM02201/22/2024
Labeler - Church & Dwight Co., Inc. (001211952)

Revised: 12/2023
Document Id: f1bb7353-1e86-409d-bb17-a93c3bfa6133
Set id: cc0c533c-145e-4877-b421-1baf3a3a572e
Version: 1
Effective Time: 20231201
 
Church & Dwight Co., Inc.