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Tartar control - Medication Information

Product NDC Code 41250-855
Drug Name

Tartar control

Type Brand
Active Ingredients
Eucalyptol .92 mg/ml
Menthol .42 mg/ml
Methyl salicylate .6 mg/ml
Thymol .64 mg/ml
Route ORAL
Dosage Form MOUTHWASH
RxCUI drug identifier 1043619
Application Number 505G(a)(3)
Labeler Name Meijer Distribution, Inc
Packages
Package NDC Code Description
41250-855-86 1000 ml in 1 bottle, plastic (41250-855-86)
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Adverse reactions

Information about undesirable effects, reasonably associated with use of the drug, that may occur as part of the pharmacological action of the drug or may be unpredictable in its occurrence. Adverse reactions include those that occur with the drug, and if applicable, with drugs in the same pharmacologically active and chemically related class. There is considerable variation in the listing of adverse reactions. They may be categorized by organ system, by severity of reaction, by frequency, by toxicological mechanism, or by a combination of these.
Adverse Reactions DISTRIBUTED BY MEIJER DISTRIBUTION, INC GRAND RAPIDS, MI 49544 www.meijer.com OUR QUALITY GUARANTEE The Meijer Family www.meijer.com/satisfaction how2recycle.info

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Eucalyptol 0.092% Menthol 0.042% Methyl salicylate 0.060% Thymol 0.064%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water, alcohol (21.6%), sorbitol, flavor, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, sodium saccharin, green 3

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use helps control plaque that leads to gingivitis

Purpose

Information about the drug product’s indications for use.
Purpose Antigingivitis, antiplaque

Spl product data elements

Usually a list of ingredients in a drug product.
Tartar control Eucalyptol, menthol, methyl salicylate, thymol WATER ALCOHOL SORBITOL POLOXAMER 407 BENZOIC ACID ZINC CHLORIDE SODIUM BENZOATE SUCRALOSE SACCHARIN SODIUM FD&C GREEN NO. 3 EUCALYPTOL EUCALYPTOL MENTHOL MENTHOL METHYL SALICYLATE SALICYLIC ACID THYMOL THYMOL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Principal display panel NDC 41250-855-86 meijer TARTAR CONTROL PLUS ANTISEPTIC Mouth Rinse Compare to Listerine ® Ultraclean ® Cool Mint ® Active Ingredients Antigingivitis/Antiplaque Blue Mint Helps fight tartar build-up Kills germs that cause bad breath, plaque and gingivitis Long lasting clean feel 33.8 FL OZ (1.05 QT) 1 L mm01

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Disclaimer *This product {or product name} is not manufactured or distributed by Kenvue, Inc., distributor of Listerine ® Ultraclean ® Cool Mint ® Antiseptic Mouthwash

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
TEP SEALED WITH A PRINTED NECKBAND FOR YOUR PROTECTION

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a dentist if gingivitis, bleeding, or redness persists for more than 2 weeks.

Storage and handling

Information about safe storage and handling of the drug product.
Other information cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-86°F)

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For this product

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API