Label: EQUALINE MULTI-ACTION ANTISEPTIC- cetylpyridinium chloride rinse
- NDC Code(s): 41163-299-86
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 17, 2026
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Tamper Evident Statement
- Claims
- 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
- Disclaimers
- ADVERSE REACTION
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Principal display panel
compare to Crest ®Pro-Health ®Alcohol Free Rinse active ingredient*
EQUALINE ®
multi-action
alcohol-free
antiseptic rinse
antigingivitis/antiplaque
mouth rinse
- kills germs that cause plaque, gingivitis, and bad breath
- helps prevent plaque
- helps prevent gingivitis
- helps keep teeth feeling clean
- freshens breath
- no burn of alcohol
fresh mint
33.8 FL OZ (1.05 QT) 1 L


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INGREDIENTS AND APPEARANCE
EQUALINE MULTI-ACTION ANTISEPTIC
cetylpyridinium chloride rinseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-299 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE 0.7 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) POLOXAMER 407 (UNII: TUF2IVW3M2) SACCHARIN SODIUM (UNII: SB8ZUX40TY) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) WATER (UNII: 059QF0KO0R) BENZOIC ACID (UNII: 8SKN0B0MIM) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-299-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/15/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 05/01/2007 Labeler - United Natural Foods, Inc. dba UNFI (943556183) Registrant - Nice-Pak Products, LLC (119091520) Establishment Name Address ID/FEI Business Operations Nice-Pak Products, LLC 119091514 manufacture(41163-299)
