Label: TARTAR CONTROL PLUS- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 55301-326-86
- Packager: Your Military Exchanges
- 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.
Drug Label Information
Updated April 1, 2022
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- Official Label (Printer Friendly)
- claims
- active ingredients
- 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 twice a day for 30 second 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
- Disclaimer
- Adverse Reactions
-
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Compare to
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Fresh Citrus
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TARTAR CONTROL
PLUS
ANTIGINGIVITIS/ANTIPLAQUE MOUTHRINSE
- Kills germs that cause bad breath, plaque & gingivitis
- Controls tartar that can discolor teeth
- Long lasting clean feeling
- Fresh breath with mouth-cooling sensation
1 L (33.8 FL OZ)
quality value
-
INGREDIENTS AND APPEARANCE
TARTAR CONTROL PLUS
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55301-326 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 0.60 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) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55301-326-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/25/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 10/25/1999 Labeler - Your Military Exchanges (001695568) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(55301-326) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(55301-326)