ATTITUDE ADULT FLUORIDE-FREE - SENSITIVE - SPEARMINT- potassium nitrate gel, dentifrice

Attitude Adult Fluoride-free - Sensitive - Spearmint by

Drug Labeling and Warnings

Attitude Adult Fluoride-free - Sensitive - Spearmint by is a Otc medication manufactured, distributed, or labeled by Attitude DBA 9055-7588 Québec Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS

Medicinal ingredient

Potassium nitrate (5% w/w)

Purpose

Anti-hypersensitivity

Uses

• Builds protection against sensitivity of the teeth.
• Shields and soothes dental nerves for lasting sensitivity relief when used regularly.

Warnings

Keep out of reach of children.

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

STOP USE

Sensitive teeth may indicate a serious problem. Stop use and consult a health care professional ifsymptoms persist or worsen.

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 or health care professional. Not recommended for children under 12 years of age. Store at room temperature (15-30 °C).

Non-medicinal ingredients

Aqua / Water / Eau, Sorbitol, Hydrated Silica, Glycerin, Sodium Methyl Cocoyl Taurate, Gaultheria Procumbens (Wintergreen) Leaf Oil, Xanthan Gum, Sodium Chloride, Citric Acid, Rebaudioside A, Sodium Benzoate, 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

fluoride free

toothpaste

Spearmint
SENSITIVE
Super Leaves

NPN 80109941

120 g / 4.2 OZ.

INGREDIENTS AND APPEARANCE

ATTITUDE ADULT FLUORIDE-FREE - SENSITIVE - SPEARMINT 
potassium nitrate gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61649-743
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
METHYL SALICYLATE (UNII: LAV5U5022Y)
XANTHAN GUM (UNII: TTV12P4NEE)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
REBAUDIOSIDE A (UNII: B3FUD0528F)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CARICA PAPAYA LEAF (UNII: 66J7636Z2I)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61649-743-01	120 g in 1 TUBE; Type 0: Not a Combination Product	06/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	06/01/2022

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

Establishment
Name	Address	ID/FEI	Business Operations
9055-7588 Québec Inc. DBA Attitude		204307099	manufacture(61649-743) , label(61649-743) , pack(61649-743) , analysis(61649-743)