Label: TARTAR CONTROL PLUS- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 30142-855-12
- Packager: The Kroger Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist if
- Keep out of reach of children.
-
Directions
adults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds 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
- this rinse is not intended to replace brushing or flossing
- Other information
- Inactive ingredients
- Questions?
-
SPL UNCLASSIFIED SECTION
DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OH 45202
QUESTIONS OR COMMNETS
1-800-632-6900 WWW. KROGER.COM
Our Brands. Our Guarantee.
Love It or Your Money Back.
www.kroger.com
*Listerine® Ultraclean™ With Everfresh™
Technology Cool Mint® is a registered trademark
of Johnson & Johnson Healthcare Products.
Johnson & Johnson Healthcare Products is not
affiliated with The Kroger Co. or this product.
DSP-TN-21091
DSP-MO-20087
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principal display panel
Compare to
Listerine® Ultraclean™ With
Everfresh™ Technology Cool Mint®
Kroger
Blue Mint
Tartar Control +
Antiseptic Mouth Rinse
ANTIGINGIVITIS/ANTIPLAQUE Mouth Rinse
KILLS GERMS THAT CAUSE BAD BREATH
PLAQUE 7 THE GUM DISEASE GINGIVITIS
LONG LASTING CLEAN FEEL
GRESH BREATH WITH MOUTH-COOLING SENSATION
CONTROLS TARTAR THAT CAN DISCOLOR TEETH
HELPS FIGHT TARTAR BUILD-UP
1.5 l (50.7 FL OZ)
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INGREDIENTS AND APPEARANCE
TARTAR CONTROL PLUS
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-855 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL 0.92 mg in 1 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.42 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.6 mg in 1 mL THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 0.64 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) ZINC CHLORIDE (UNII: 86Q357L16B) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) SACCHARIN SODIUM (UNII: SB8ZUX40TY) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-855-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/14/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/14/2022 Labeler - The Kroger Co. (006999528) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(30142-855)