Dentalux 664.003/664AT rev 2 664AU

Manufacturer
Lidl US, LLC | Nice-Pak Products, LLC
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
21
Source
daily-update
Hydrated at
2026-08-08 02:02:14

Label at a glance#

ProductAntispetic
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 twice a day for 30 seconds then spit out; do not swallow children under 12 years of age - consult a dentist or doctor 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 twice a day for 30 seconds then spit out; do not swallow

children under 12 years of age - consult a dentist or doctor

  • 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°-77°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol 21.6%, sorbitol, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, flavor, green 3

Questions or comments?

OTC - QUESTIONS SECTION

1-844-344-5071

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Kenvue, Inc., distributor of Cool Mint  Listerine ® Antiseptic Mouthwash.

Adverse Reaction

ADVERSE REACTIONS SECTION

DISTRIBUTED BY LIDL US, LLC

ARLINGTON, VA 22202

QUESTIONS? 1-844-344-5071

www.lidl.com

LiDL Love it! Guarantee

  • money refunded
  • item replaced

save water.lidl

Discard Seal, Empty & Replace Cap

PLASTIC BOTTLE

how2recycle.info

DSP-TN-21091 DSP-MO-20087

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dentalux by LiDL  ®

BLUE MINT

ANTI-GINGIVITIS/ANTI-PLAQUE MOUTHWASH

ANTISEPCTIC MOUTHWASH

ADA ACCEPTED

American Dental Association  ®

  • Helps prevent and reduce plaque
  • Helps prevent and reduce gingivitis

SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

Kills Germs that Cause Plaque, Gingivitis, Bad Breath

NDC 71141-156-12

50.7 FL OZ (1.58 QT) 1.5 L

image descriptionimage descriptionimage descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71141-15671141-156-32, 71141-156-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
202026-02-04full-release2026-06-01 01:36:58

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
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLLidl US, LLCaf0bda7c-591f-4451-bb47-b83c2b4193722026-08-05Warnings, Adverse reactionsExact identifier
ndc (package): 71141-156-12
ndc (package): 71141-156-32
ndc (product): 71141-156
ndc11 (package): 71141015632
ndc11 (package): 71141015612
spl id: 584d8efe-0421-9966-e063-6394a90a8932
spl set id: af0bda7c-591f-4451-bb47-b83c2b419372

Reported adverse events (FAERS/openFDA)#

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