Quality choice mint liquid

Active ingredients

Cetylpyridinium Chloride 0.07%

Purpose

Antiplaque/Antigingivitis

Uses

  • Helps reduce and prevent plaque and gingivitis.
  • Helps control plaque bacteria that contribute to the development of gingivitis and bleeding gums.

Warnings

Ask dentist if symptoms persist or condition worsens after regular use.

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 immediately (1-800-222-1222)

Directions

  • Use after your normal brushing and flossing routine; rinse toothpaste from mouth prior to use
  • Adults and children 6 years and older:Rinse for 30 seconds with 20 mL (4 teaspoonfuls) twice a day.
  • Do not swallow
  • Children 6 years to under 12 years of age: supervise use
  • Children under 6 years of age: do not use.

Other information

Store at room temperature

Inactive ingredients

Water (Aqua), Glycerin, Poloxamer 407, Flavor, Sodium Saccharin, Methylparaben, Sucralose, Propylparaben, Blue 1 (CI 42090)

Questions or comments?

1-248-449-9300

Ingredients and appearance - Product information

Quality choice mint liquid- Cetylpryidinium chloride

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 63868-553
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Cetylpyridinium chloride ( UNII: D9OM4SK49P)( Cetylpyridinium - UNII: CUB7JI0JV3 ) 0.7 mgin 1 mL

Inactive Ingredients

Ingredient Name Code
Water ( UNII: 059QF0KO0R)
Glycerin ( UNII: PDC6A3C0OX)
Poloxamer 407 ( UNII: TUF2IVW3M2)
Saccharin sodium ( UNII: SB8ZUX40TY)
Methylparaben ( UNII: A2I8C7HI9T)
Sucralose ( UNII: 96K6UQ3ZD4)
Propylparaben ( UNII: Z8IX2SC1OH)
Fd&c blue no. 1 ( UNII: H3R47K3TBD)

Product Characteristics

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part356 USA

Labeler - CHAIN DRUG MARKETING ASSOCIATION INC( 011920774)

Establishment

Name ID/FEI Business Operations
CHAIN DRUG MARKETING ASSOCIATION INC 011920774 manufacture( 63868-553)

Label copy