DRUG FACTS

Active ingredient

Sodium fluoride (0.243% w/w)

Purpose

Anti-cavity

Uses

Prevents, fights and protects against cavities and tooth decay.
Effective fluoride protection.
Protects teeth from acid erosion.
Penetrates tooth enamel to help rebuild weak spots.

Warnings

Keep out of reach of children.

If swallowed, call a poison control centre or get medical help right away.

Directions

Do not swallow. Should be used as part of an oral health program that includes regular flossing and dental check-ups. Brush teeth thoroughly for at least 1 minute twice a day, preferably after each meal, or as directed by a dentist. Children under 6 years of age should use only a pea-sized amount and be supervised to brush properly and to not swallow. Consult a dentist or health care professional before using with children under 2 years of age.

Inactive ingredients / Ingrédients inactifs : Aqua / Water / Eau, Sorbitol, Glycerin, Hydrated Silica, Sodium Lauryl Sulfate, Gaultheria Procumbens (Wintergreen) Leaf Oil, Xanthan Gum, Citric Acid, Rebaudioside A, Sodium Benzoate, Sodium Bicarbonate, Potassium Sorbate, Carica Papaya (Papaya) Leaf Extract, Camellia Sinensis (Tea) Leaf Extract.

QUESTIONS?

Questions? +1-855-509-7225

PRINCIPAL DISPLAY PANEL - 120 g Tube Label

ATTITUDE ®

natural care

EWG Verified

Vegan

with fluoride

toothpaste

Spearmint
ENAMEL CARE
Super leaves TM

NPN 80104880

120 g / 4.2 OZ.

Label

BIO SPECTRA ATTITUDE
sodium fluoride gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:61649-734
Route of Administration	DENTAL

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

Ingredient Name	Strength
Inactive Ingredients
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
METHYL SALICYLATE (UNII: LAV5U5022Y)
XANTHAN GUM (UNII: TTV12P4NEE)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
REBAUDIOSIDE A (UNII: B3FUD0528F)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CARICA PAPAYA LEAF (UNII: 66J7636Z2I)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Product Characteristics
Color	white (Opaque)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:61649-734-01	120 g in 1 TUBE; Type 0: Not a Combination Product	05/15/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M021	05/15/2021

Labeler - 9055-7588 Québec Inc. DBA ATTITUDE (201137051)

Name	Address	ID/FEI	Business Operations
Establishment
9055-7588 Québec Inc. DBA ATTITUDE		204307099	manufacture(61649-734) , label(61649-734) , pack(61649-734) , analysis(61649-734)