DENTALUX ANTI-CAVITY FLUORIDE WHITENING MINT- sodium fluoride paste, dentifrice

dentalux ANTI-CAVITY FLUORIDE WHITENING MINT by

Drug Labeling and Warnings

dentalux ANTI-CAVITY FLUORIDE WHITENING MINT by is a Otc medication manufactured, distributed, or labeled by Lidl US, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Sodium Fluoride
0.243 % (0.15 % w/v Fluoride ion)

Purpose

Anticavity

Uses

helps protect against cavities.

Warnings

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist.
do not swallow.
children 2 to 6 years: to minimize swallowing use a pea-sized amount and supervise children's brushing and rinsing until good habits are established.
children under 2 years of age: Consult a dentist or doctor.

Inactive ingredients

Sorbitol, Treated Water (Aqua), Hydrated Silica, PEG-1500, Sodium Lauryl Sulphate, Flavor, Cellulose Gum, Tetrasodium Pyrophosphate, Benzyl Alcohol, Sodium Saccharin, Carbomer, Sodium Hydroxide, Mica, Titanium Dioxide, FD&C Blue 1.

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

*COMPARE TO Crest® 3D White™ Radiant Mint

FIGHTS TARTAR

ENAMEL SAFE WHITENING

GIVES YOU A FLAWLESS BRIGHT AND WHITE SMILE

DISTRIBUTED BY LIDL US, LLC
ARLINGTON, VA 22202
PRODUCT OF INDIA
1-844-344-5071

*THIS PRODUCT IS NOT MANUFACTURED OR DISTRIBUTED BY THE PROCTER & GAMBLE COMPANY, OWNER OF THE REGISTERED TRADEMARKS CREST® AND 3D WHITE™.

Packaging

INGREDIENTS AND APPEARANCE

DENTALUX ANTI-CAVITY FLUORIDE WHITENING MINT 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71141-185
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.243 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71141-185-10	1 in 1 BOX	06/30/2024
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	06/30/2024

Labeler - Lidl US, LLC (079389709)