Tartar control plus

Manufacturer
United Natural Foods, Inc. dba UNFI | Consumer Product Partners, LLC
Effective date
2024-09-13
Label type
HUMAN OTC DRUG LABEL
Version
15
Source
legacy-cache
Hydrated at
2026-08-01 20:54:57

Label at a glance#

ProductTartar control plus
Active ingredientEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
Label structure14 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Eucalyptol 0.092%

Menthol 0.042%

Methyl salicylate 0.060%

Thymol 0.064%

Purpose

OTC - PURPOSE SECTION

Antigingivitis, Antiplaque

Use

INDICATIONS & USAGE SECTION

helps control plaque that leads to gingivitis

Warnings

WARNINGS SECTION

for this product

Do not use

OTC - DO NOT USE SECTION

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.

Stop use and ask a dentist if

OTC - STOP USE SECTION

gingivitis, bleeding, or redness persists for more than 2 weeks.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

SPL UNCLASSIFIED SECTION

cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

 water, alcohol (21.6%), sorbitol, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, flavor, sodium saccharin, blue 1

TEP

OTHER SAFETY INFORMATION

Sealed With Printed Neckband For Your Protection

Disclaimer

SPL UNCLASSIFIED SECTION

This product is not manufactured or distribted by Johnson & Johnson Healthcare Products, distributor of Listerine Ultraclean With Everfresh Technology - Artic Mint.

Adverse Reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY SUPERVALU INC.

EDEN PRAIRIE, MN 55344 USA

Contact us at 1-877-932-7948,

or www.supervalu-ourownbrands.com

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Listerine Ultraclean Arctic Mint active ingredents*

EQUALIME

tartar control plus

antiseptic

mouthrinse

antigingivitis/antiplaque

  • kills germs that cause bad breath, plaque & the gum disease gingivitis

iceberg blue

1L (33.8 FL OZ)

image descriptionimage description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-01541163-015-86

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24c623d7-b68b-65ee-e063-6394a90a92711086ecff-7a5a-4291-83f7-cc871ddd13b02024-10-18Warnings, Adverse reactionsExact identifier
spl set id: 1086ecff-7a5a-4291-83f7-cc871ddd13b0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.