ATTITUDE ADULT FLUORIDE-FREE - SENSITIVE - SPEARMINT- potassium nitrate gel, dentifrice
Attitude DBA 9055-7588 Québec Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Attitude® Adult Fluoride-free Toothpaste - Sensitive - Spearmint

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.

Sensitive teeth may indicate a serious problem. Stop use and consult a health care professional if symptoms 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

Sorbitol, aqua, glycerin, hydrated silica, sodium methyl cocoyl taurate, gaultheria procumbens (wintergreen) leaf oil1, xanthan gum, citric acid, stevia rebaudiana leaf/stem extract, sodium benzoate, carica papaya (papaya) leaf extract, camellia sinensis (green tea) leaf extract, potassium sorbate, sodium chloride.

1: Naturally contains : D-limonene.

QUESTIONS?

+1 (514) 509-7225

PRINCIPAL DISPLAY PANEL - 120 g Tube Label

ATTITUDE®
bio spectra
natural care

toothpaste • fluoride free

toothpaste
SENSITIVE
Spearmint • Fluoride free

ECO-CONSCIOUS

• EWG VERIFIED •
FOR YOUR HEALTH • EWG.ORG

VEGAN

NPN 80109941

GEL • 120 g e 4.2 OZ.

PRINCIPAL DISPLAY PANEL - 120 g Tube Label

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

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

Ingredient Name	Strength
Inactive Ingredients
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)
STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
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

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

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part356	06/01/2022

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

Name	Address	ID/FEI	Business Operations
Establishment
Attitude DBA 9055-7588 Québec Inc.		204307099	MANUFACTURE(61649-743) , LABEL(61649-743) , PACK(61649-743) , ANALYSIS(61649-743)

Name	Address	ID/FEI	Business Operations
Establishment
Attitude DBA 9055-7588 Québec Inc.		201137051	MANUFACTURE(61649-743) , ANALYSIS(61649-743)

Revised: 6/2022

Document Id: 70381f77-2cd9-404c-9f99-a3a79643f456

Set id: 46d5c908-f0e3-444c-9d96-461feef39137

Version: 1

Effective Time: 20220602

Attitude DBA 9055-7588 Québec Inc.