PARODONTAX  ACTIVE GUM REPAIR BREATH FRESHENER- stannous fluoride paste 
Haleon US Holdings LLC

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Drug Facts

Active ingredient

Stannous fluoride 0.454% (0.15% w/v fluoride ion)

Purposes

Anticavity

Antigingivitis

Uses

Warnings

Stop use and ask a dentist if

  • gingivitis, bleeding, or redness persists for more than 2 weeks.
  • you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease

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

Other information

Inactive ingredients

glycerin, PEG-8, hydrated silica, pentasodium triphosphate, flavor, sodium lauryl sulfate, titanium dioxide, polyacrylic acid, cocamidopropyl betaine, sodium saccharin, zinc chloride, carrageenan

Questions or comments?

1-855-328-5202

Additional information

ALWAYS FOLLOW THE LABEL

parodontax ACTIVE GUM REPAIR
Bleeding gums and bad breath can be a sign of early gum problems.

New parodontax Active Gum RepairBreath Freshener is a daily toothpaste that helps reverse signs of early gum damage and uses Breath Cleanse Technology* to purify bad breath instead of just masking it.

*compared to parodontax Clean Mint toothpaste

Distributed by:

GSK Consumer Healthcare

Warren, NJ 07059 Made in Germany

Trademarks owned or licensed by GSK. ©2023 GSK or licensor.

Principal Display Panel

NEW

parodontax

DAILY FLUORIDE ANTICAVITY AND ANTIGINGIVITIS TOOTHPASTE

ACTIVE GUM REPAIR

HELPS REVERSE SIGNS OF EARLY GUM DAMAGE

BREATH FRESHENER

BREATH CLEANSE TECHNOLOGY*

NET WT 3.4 OZ (96.4 g)

62000000203673 – Front Carton

Parodontax Active Gun Repair BF 3.4 oz (96.4 g)
PARODONTAX   ACTIVE GUM REPAIR BREATH FRESHENER
stannous fluoride paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0737
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
CARRAGEENAN (UNII: 5C69YCD2YJ)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0737-011 in 1 CARTON01/02/2024
196.4 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0135-0737-021 in 1 CARTON01/02/2024
223 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02201/02/2024
Labeler - Haleon US Holdings LLC (079944263)

Revised: 2/2024
Document Id: 10f3f7bc-1355-dd53-e063-6394a90acbbd
Set id: addcb1e2-24b9-4367-adf3-6806e2439a80
Version: 3
Effective Time: 20240209
 
Haleon US Holdings LLC