EVO ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT- sodium fluoride paste, dentifrice

evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT by

Drug Labeling and Warnings

evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT by is a Otc medication manufactured, distributed, or labeled by Ashtel Studios, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Sodium Fluoride 0.24%
(0.17% w/v Fluoride ion)

Purpose

Anticavity

Uses

helps in the prevention of dental decay

Warnings

Do not use if you are allergic to any of the ingredients.

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

Do not swallow

Supervise children as necessary until capable of using without supervision

Adult and children 2 years and older
   brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician

Children under 6 years
   instruct in good brushing and rinsing habits (to minimize swallowing)

Children under 2 years
   ask a dentist or physician

Inactive ingredients

Calcium Carbonate, Aqua (Water), Sorbitol, Silica, Sodium Lauryl Sulfate, Flavor, Sodium Bicarbonate, Benzyl Alcohol, PEG-8, Cellulose Gum, Xanthan Gum, Sodium Saccharin, Sodium Benzoate, Titanium Dioxide, Sodium Silicate

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

HELPS FIGHT CAVITIES
GENTLY CLEAN TEETH
CLEAN FRESH BREATH
STRENGTHEN ENAMEL
REMOVES STAINS & PLAQUE

DESIGNED IN U.S.A.
MADE IN INDIA

GETEVO.NET

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE
DISTRIBUTED BY ASHTEL STUDIOS INC., ONTARIO, CALIFORNIA 91761

Packaging

INGREDIENTS AND APPEARANCE

EVO ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-204
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.24 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZYL ALCOHOL (UNII: LKG8494WBH)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
XANTHAN GUM (UNII: TTV12P4NEE)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM SILICATE (UNII: IJF18F77L3)

Product Characteristics
Color		Score
Shape		Size
Flavor	PEPPERMINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-204-01	1 in 1 BOX	06/30/2025
1		99 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	06/30/2025

Labeler - Ashtel Studios, Inc. (148689180)