Label: SMARTMOUTH SMARTMOUTH GUM HEALTH ZINC ACTIVATED FORMULA- cetylpyridinium chloride kit
- NDC Code(s): 76357-509-01, 76357-599-02
- Packager: Triumph Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
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Directions
- Use after your normal brushing and flossing routine
- Adults and children 12 years of age & older: vigorously swish 20 mL of rinse (pour to indicator line on cap) twice a day for 30 seconds and then spit out. Do not swallow.
- Children 6 years to under 12 years of age: supervise use.
- Children under 6 years of age: do not use unless directed by a healthcare professional.
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Inactive Ingredients
Solution 1: Purified Water, Sodium Benzoate, Sodium Chlorite, and Benzoic Acid. Solution 2: Purified Water, Glycerin, Poloxamer 407, Propylene Glycol, Aloe Vera, Poloxamer 124, Zinc Chloride, Flavor, Sodium Benzoate, Benzoic Acid, Sodium Saccharin, Sodium Chloride, Benzyl Alcohol, D&C Yellow No. 10, FD&C Blue No. 1
- Questions?
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - Kit Label
NEW &
IMPROVED
POURMIXES TO
ACTIVATE
2 Powerful SolutionsBLOCKS
ODORS
FRESHENS
BREATHsmart
mouth™Gum Health
Scientifically Proven
Smart-Zinc™ Technology24
HOURBAD BREATH
PREVENTION
WITH A MORNING & EVENING RINSEAdvanced Germ Killing+
BLEEDING GUMS PROTECTION
SOOTHES WITH NATURAL ALOEMILD MINT • 16 FL. OZ. (473 mL) • ALCOHOL FREE
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INGREDIENTS AND APPEARANCE
SMARTMOUTH SMARTMOUTH GUM HEALTH ZINC ACTIVATED FORMULA
cetylpyridinium chloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76357-509 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76357-509-01 1 in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2024 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 237 mL Part 2 1 BOTTLE 237 mL Part 1 of 2 SMARTMOUTH GUM HEALTH SOLUTION 1
mouthwashes and breath fresheners (liquids and sprays) [oral products] liquidProduct Information Route of Administration DENTAL Other Ingredients Ingredient Kind Ingredient Name Quantity INGR Water (UNII: 059QF0KO0R) INGR Sodium Benzoate (UNII: OJ245FE5EU) INGR Sodium Chlorite (UNII: G538EBV4VF) INGR Benzoic Acid (UNII: 8SKN0B0MIM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 237 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date COSMETIC 01/01/2024 Part 2 of 2 SMARTMOUTH GUM HEALTH SOLUTION 2
cetylpyridinium chloride liquidProduct Information Item Code (Source) NDC:76357-599 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Cetylpyridinium Chloride (UNII: D9OM4SK49P) (Cetylpyridinium - UNII:CUB7JI0JV3) Cetylpyridinium Chloride 500 mg in 20 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Poloxamer 407 (UNII: TUF2IVW3M2) Propylene Glycol (UNII: 6DC9Q167V3) ALOE (UNII: V5VD430YW9) POLOXAMER 124 (UNII: 1S66E28KXA) Zinc Chloride (UNII: 86Q357L16B) SODIUM (UNII: 9NEZ333N27) Benzoic Acid (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Sodium Chloride (UNII: 451W47IQ8X) Benzyl Alcohol (UNII: LKG8494WBH) Product Characteristics Color GREEN Score Shape Size Flavor MINT (Mild Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76357-599-02 237 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 01/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 01/01/2024 Labeler - Triumph Pharmaceuticals, Inc. (017853461)