PARODONTAX  ACTIVE GUM HEALTH MINT- cetylpyridinium chloride mouthwash 
PARODONTAX  ACTIVE GUM HEALTH CLEAR MINT- cetylpyridinium chloride mouthwash 
Haleon US Holdings LLC

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Drug Facts

Active ingredient

Cetylpyridinium chloride 0.07% w/w

Purpose

Antigingivitis, Antiplaque

Uses

Warnings

Stop use and ask a dentist if

  • irritation occurs
  • 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 rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients (Mint)

Water, glycerin, flavor, poloxamer 188, sodium saccharin, propylene glycol, sodium benzoate, sucralose, benzoic acid, blue 1

Inactive Ingredients (Clear Mint)

Water, glycerin, flavor, poloxamer 188, sodium saccharin, propylene glycol, sodium benzoate, sucralose, benzoic acid

Questions or comments?

1-855-328-5202

Additional Information

*Kills plaque bacteria associated with gingivitis and odor-causing bacteria in a laboratory test

Do not use if the printed seal on the cap is broken or missing.

ALWAYS FOLLOW THE LABEL

Distributed by: GSK Consumer Healthcare,Warren, NJ 07059

Trademarks are owned by or licensed to the GSK group of companies.

©2022 GSK group of companies or its licensor.

1-855-328-5202

Principal Display Panel

NDC 0135-0651-02

NEW

parodontax

CETYLPYRIDINIUM CHLORIDE ANTIGINGIVITIS/
ANTIPLAQUE MOUTHRINSE

ACTIVE GUM HEALTH
DAILY MOUTHWASH

TARGETS BACTERIA*
& FORMS AN
ANTIBACTERIAL SHIELD

MINT

KILLS 99.9%
PLAQUE
BACTERIA*

16.9 FL OZ (500 mL)

L0020006FA: Front Label

L0020006BA: Back Label

parodontax active gum health mouthwash mint

Principal Display Panel

NDC 0135-0650-01

NEW

parodontax

CETYLPYRIDINIUM CHLORIDE ANTIGINGIVITIS/
ANTIPLAQUE MOUTHRINSE

ACTIVE GUM HEALTH

DAILY MOUTHWASH

TARGETS BACTERIA*
& FORMS AN
ANTIBACTERIAL SHIELD

CLEAR MINT

DYE FREE
ALCOHOL FREE

16.9 FL OZ (500 mL)

L0020007FA: Front Label

L0020007BA: Back Label

parodontax active gum health mouthwash clear mint
PARODONTAX   ACTIVE GUM HEALTH MINT
cetylpyridinium chloride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0651
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLOXAMER 188 (UNII: LQA7B6G8JG)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
2,3'-IMINODI-BENZOIC ACID (UNII: H1C37ZB0P3)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0651-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2022
2NDC:0135-0651-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02201/03/2022
PARODONTAX   ACTIVE GUM HEALTH CLEAR MINT
cetylpyridinium chloride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0650
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.7 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLOXAMER 188 (UNII: LQA7B6G8JG)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0650-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02201/03/2022
Labeler - Haleon US Holdings LLC (079944263)

Revised: 2/2024
Document Id: 10f312da-beeb-930c-e063-6294a90a9656
Set id: 444f931d-5e38-4cda-97ba-98aa0b5fe4f6
Version: 3
Effective Time: 20240209
 
Haleon US Holdings LLC