Label: ANTISEPTIC- cetylpyridinium chloride rinse
- NDC Code(s): 0869-0299-86
- Packager: Vi-Jon, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated August 5, 2022
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- Active ingrediet
for this product
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 gun line, loose teeth or increased spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease.
- Other information
- inactive ingredients
SPL UNCLASSIFIED SECTION
Alcohol-Free ANTISEPTIC RINSE
For better oral hygiene and fresher breath
This rinse may cause temporary staining to the surface of teeth. This is not harmful, and adequate brushing may prevent its occurence.
*This product is not manufactured or distributed by Procter & Gamble, distributor of Crest Pro-Health Multi-Protection Alcohol Free Rinse - Refreshing Clean Mint
Distributed by: Vi-Jon, LLC., St. Louis, MO 63114
principal display panel
Sealed with printed neckband for your protection
Helps prevent plaque
Helps prevent gingivitis
Helps keep teeth feeling clean
No burn of alcohol
Compare to Crest Pro-health Multi Protection Alcohol Free Rinse Refreshing Clean Mint*
1 LITER (33.8 FL OZ)
INGREDIENTS AND APPEARANCE
cetylpyridinium chloride rinse
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0299 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE 0.07 kg in 100 L Inactive Ingredients Ingredient Name Strength 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) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0869-0299-86 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/05/1995 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 01/05/1995 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0299) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(0869-0299)