ACT TOTAL CARE DRY MOUTH ANTICAVITY MOUTH- sodium fluoride rinse 
Chattem, Inc.

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ACT Total Care Anticavity Fluoride Rinse Dry Mouth

Drug Facts

Active ingredient

Sodium fluoride 0.02% (0.009% w/v fluoride ion)

Purpose

Anticavity

Use

Warnings

Keep out of 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 6 years of age and older:

children under 6 years of age: consult a dentist or doctor

Other information

Inactive ingredients

water, glycerin, sorbitol, xylitol, poloxamer 407, betaine, propylene glycol, flavors, bisabolol, carnosine, PEG-14M, PEG-160M, zingiber officinale (ginger) root extract, angelica polymorpha sinensis root extract, lonicera japonica (honeysuckle) flower extract, pueraria lobata root extract, sodium benzoate, potassium sorbate, sodium phosphate, disodium phosphate, polysorbate 20, lactic acid, calcium disodium EDTA, cetylpyridinium chloride, sucralose, green 3, yellow 10 (309-043)

Learn more at www.ACTFLUORIDE.com

PRINCIPAL DISPLAY PANEL

#1 DENTIST RECOMMENDED
FLUORIDE BRAND
ACT
® TOTAL CARE
ANTICAVITY FLUORIDE RINSE
DRY MOUTH
 SOOTHES Dry Mouth
 MOISTURIZES Mouth Tissue
 STRENGTHENS Teeth
 FRESHENS Breath
Sodium Fluoride 0.02%
18 fl oz (532 mL)

PRINCIPAL DISPLAY PANEL
#1 DENTIST RECOMMENDED 
FLUORIDE BRAND
ACT® TOTAL CARE 
ANTICAVITY FLUORIDE RINSE 
DRY MOUTH
● SOOTHES Dry Mouth
● MOISTURIZES Mouth Tissue
● STRENGTHENS Teeth
● FRESHENS Breath
Sodium Fluoride 0.02%
18 fl oz (532 mL)
PRINCIPAL DISPLAY PANEL
#1 DENTIST RECOMMENDED 
FLUORIDE BRAND
ACT® TOTAL CARE 
ANTICAVITY FLUORIDE RINSE 
DRY MOUTH
● SOOTHES Dry Mouth
● MOISTURIZES Mouth Tissue
● STRENGTHENS Teeth
● FRESHENS Breath
Sodium Fluoride 0.02%
18 fl oz (532 mL)

ACT TOTAL CARE DRY MOUTH ANTICAVITY MOUTH 
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0968
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.09 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
XYLITOL (UNII: VCQ006KQ1E)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
BETAINE (UNII: 3SCV180C9W)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LEVOMENOL (UNII: 24WE03BX2T)  
CARNOSINE (UNII: 8HO6PVN24W)  
GINGER (UNII: C5529G5JPQ)  
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
PUERARIA MONTANA VAR. CHINENSIS ROOT (UNII: FQN0D1U235)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
LACTIC ACID (UNII: 33X04XA5AT)  
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0968-588 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2011
2NDC:41167-0968-0532 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2011
3NDC:41167-0968-31000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2011
4NDC:41167-0968-930 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/01/2011
Labeler - Chattem, Inc. (003336013)

Revised: 10/2023
Document Id: e05fddfa-05a2-44c0-a7a7-2436f1b9ddc1
Set id: 06684b82-aaa0-4ca6-8d56-4f9866269000
Version: 11
Effective Time: 20231020
 
Chattem, Inc.