GURUNANDA SENSITIVE- potassium nitrate paste

GuruNanda Sensitive by

Drug Labeling and Warnings

GuruNanda Sensitive by is a Otc medication manufactured, distributed, or labeled by GURUNANDA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Potassium nitrate 5%

Purpose

Antihypersensitivity

Use

Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact

Warnings

Warnings

When using this product

if pain/sensitivity still persists after 4 weeks of use, stop use and contact your dentist.

Stop use and ask a dentist

if the problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist.

Keep out of reach of children.

If more than used for brusing is accidently swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Directions

Adults and children 12 years of age and older:

• Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (mroning and evening) or as recommended by a dentist or doctor.
• Make sure to brush all sensitive areas of the teeth.

Children under 12 years of age:

• Consult a dentist or doctor

Other information

Do not use if the foil seal on the tube is broken or missing

Inactive ingredients

Water, Glycerin, Hydrated Silica, Xylitol, Sorbitol, Calcium Hydroxyapatite, Cocamidopropyl Betaine, Sodium Cocoyl Glutamate, Xanthan Gum, Stevia Leaf Extract, Natural Flavor, D-Alpha Tocopherol, Sodium Bicarbonate, Menthol, Wintergreen Oil, Arginine, Celtic Sea Salt, White Turmeric Oil, Eucalyptus Oil, Clove Oil, Peppermint Oil, White Thyme Oil, Menaquinone-7 (Vitamin K2), Caprylic/Capric/Lauric Triglyceride

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GURUNANDA SENSITIVE 
potassium nitrate paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70708-645
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SEA SALT (UNII: 87GE52P74G)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
MENAQUINONE-7 (UNII: 8427BML8NY)
XANTHAN GUM (UNII: TTV12P4NEE)
GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OIL (UNII: LAV5U5022Y)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
TURMERIC OIL (UNII: 6KGS8SP16U)
XYLITOL (UNII: VCQ006KQ1E)
SORBITOL (UNII: 506T60A25R)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
ARGININE (UNII: 94ZLA3W45F)
STEVIA LEAF (UNII: 6TC6NN0876)
MENTHOL (UNII: L7T10EIP3A)
CALCIUM HYDROXYAPATITE (UNII: 91D9GV0Z28)
EUCALYPTUS OIL (UNII: 2R04ONI662)
WATER (UNII: 059QF0KO0R)
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
CLOVE OIL (UNII: 578389D6D0)
PEPPERMINT OIL (UNII: AV092KU4JH)
THYME OIL (UNII: 2UK410MY6B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70708-645-04	1 in 1 CARTON	09/26/2025
1		119 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	M022	09/01/2025

Labeler - GURUNANDA, LLC (079671169)