PARODONTAX  COMPLETE PROTECTION- stannous fluoride paste 
Haleon US Holdings LLC

----------

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

children under 2 years of age:Consult a dentist or doctor.

Other information

Inactive ingredients

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

Questions or comments?

Call toll-free 1-855-328-5202

ALWAYS FOLLOW THE LABEL

Additional Information

ALWAYS FOLLOW THE LABEL

Free-Sample, not for retail sale

Trademarks owned or licensed by GSK.

©2022 GSK or licensor.

Warren, NJ 07059

Principal Display Panel

DAILY FLUORIDE ANTICAVITY AND ANTIGINGIVITIS TOOTHPASTE

parodontax

HELPS PREVENT BLEEDING GUMS

PURE FRESH MINT

COMPLETE PROTECTION

SCAN TO SAVE NOW

NET WT 0.8 OZ (23 g)

62000000076142

 Parodontax Complete Protection 0.8 oz (23 g)
PARODONTAX   COMPLETE PROTECTION
stannous fluoride paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0627
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)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0627-021 in 1 CARTON11/01/2018
196.4 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0135-0627-031 in 1 CARTON01/06/2020
265.2 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:0135-0627-011 in 1 CARTON04/01/2020
323 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:0135-0627-0423 g in 1 TUBE; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02211/01/2018
Labeler - Haleon US Holdings LLC (079944263)

Revised: 2/2024
Document Id: 10f422f9-737d-1692-e063-6294a90a9a47
Set id: 59bb84d6-6fd3-4586-bccf-7dc45cbbb39c
Version: 5
Effective Time: 20240209
 
Haleon US Holdings LLC