Label: ANTIGINGIVITIS/ANTIPLAQUE- cetylpyridinium chloride mouthwash
- NDC Code(s): 76162-953-86
- Packager: TopCo Associates LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 18, 2024
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- Official Label (Printer Friendly)
- Tamper Evident Statement
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Claims & Disclaimer
QUALITY GUARANTEED
This rinse may cause temporary staining to the surface of teeth. This is not harmful, and adequate brushing may prevent its occurrence.
*This product is not manufactured or distributed by Procter & Gamble, distributor of Crest ®Pro-Health ®Intense Clean Mint Mouthwash.
**Kills at least 99% of many organisims commonly associated with bad breath in as little as 15 seconds.
- Active Ingredient
- Purpose
- Use
- Warnings
- Stop use and ask a dentist if
- Keep out of reach of children under 6 years of age.
- Directions
- Other information
- Inactive ingredients
- Questions?
- Adverse reaction
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Principal Panel Display
COMPARE TO CREST® PRO-HEALTH® INTENSE CLEAN MINT MOUTHWASH*
TopCare ® everyday
Powerful Fresh
Antigingivitis/Antiplaque
Mouthwash
FRESH MINT
Kills 99% of many bad breath germs**
Freshens your breath
Helps prevent plaque and gingivitis
IMPORTANT: Read directions for proper use.
1 L (1.5 QT) 33.8 FL OZ
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INGREDIENTS AND APPEARANCE
ANTIGINGIVITIS/ANTIPLAQUE
cetylpyridinium chloride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76162-953 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLOXAMER 407 (UNII: TUF2IVW3M2) SUCRALOSE (UNII: 96K6UQ3ZD4) BENZOIC ACID (UNII: 8SKN0B0MIM) SODIUM BENZOATE (UNII: OJ245FE5EU) CINNAMALDEHYDE (UNII: SR60A3XG0F) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76162-953-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M505G(a)(3) 04/18/2024 Labeler - TopCo Associates LLC (006935977) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(76162-953)