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Tartar control plus - Medication Information

Product NDC Code 37808-434
Drug Name

Tartar control plus

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 part356
Labeler Name HEB
Packages
Package NDC Code Description
37808-434-86 1000 ml in 1 bottle, plastic (37808-434-86)
Check if available Online

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 Section MADE WITH PRIDE AND CARE FOR H-E-B, SAN ANTONIO, TX If you aren't completely pleased with this product, we'll be happy to replace it or refund your money. You have our word on it.

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients 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, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, flavor, sodium saccharin, blue 1

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 help 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 plus Eucalyptol, menthol, methyl salicylate, thymol EUCALYPTOL EUCALYPTOL MENTHOL MENTHOL METHYL SALICYLATE SALICYLIC ACID THYMOL THYMOL WATER ALCOHOL SORBITOL POLOXAMER 407 BENZOIC ACID ZINC CHLORIDE SODIUM BENZOATE SUCRALOSE SACCHARIN SODIUM FD&C BLUE NO. 1

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 Compare to Listerine Ultraclean Arctic Mint Mouthwash H-E-B Iceberg Blue TARTAR CONTROL PLUS ANTIGINGIVITIS/ANTIPLAQUE MOUTHWASH Helps Control Plaque That Leads To Gingivitis Fights Plaque & Gingivitis Long Lasting Clean Feel Fresh Breath With Mouth Cooling Sensation 33.8 FL OZ (1 QT) 1 L image description

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.
TEP Sealed with printed neckband for your protection Other information cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-86°F) Disclaimer *This product is not manufactured or distributed by Johnson & Johnson Healthcare Products, distributor of Listerine Ultraclean With Everfresh Technology-Arctic Mint. DSP-TN-15000 DSP-MO-34 SDS-TN-15012

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
questions? call 1-888-593-0593

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.

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