MedPath

Potassium nitrate

Generic Name
Potassium nitrate
Brand Names
Meijer, Prevident 5000 Sensitive, Styptstix
Drug Type
Small Molecule
Chemical Formula
KNO3
CAS Number
7757-79-1
Unique Ingredient Identifier
RU45X2JN0Z

Overview

Potassium nitrate is an inorganic salt with a chemical formula of KNO3. It is a natural source of nitrate and has been used as a constituent for several different purposes, including food preservatives, fertilizers, tree stump removal, rocket propellants, and fireworks. Potassium nitrate is a common active ingredient in toothpaste, exerting an anti-sensitivity action. It provides increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact . In addition, potassium nitrate is used as a diuretic in pigs, cattle, and horses. It is administered orally doses up to 30 g per animal per day .

Indication

For the relief of tooth sensitivity, and is also used as a pesticide, insecticide, as a food additive, and a rodenticide .

Associated Conditions

  • Sensitivity, Tooth

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Fulijaya Manufacturing Sdn. Bhd
62776-003
DENTAL
50 mg in 1 g
6/23/2025
CHAIN DRUG MARKETING ASSOCIATION INC
63868-172
DENTAL
5 g in 100 g
8/12/2025
Colgate Oral Pharmaceuticals, Inc.
0126-0070
DENTAL
57.5 mg in 1 mL
12/9/2019
Safeway
21130-351
DENTAL
5 g in 100 g
8/12/2025
Publix Super Market
56062-413
ORAL
5 g in 100 g
8/12/2025
Westminster Pharmaceuticals, LLC
69367-318
DENTAL
57.5 mg in 1 mL
6/15/2022
Target
11673-237
DENTAL
5 g in 100 g
8/12/2025
Kroger Company
30142-362
DENTAL
5 g in 100 g
8/12/2025
The Atlanta Dental Supply Company DBA Advanced Dental Products
71347-500
ORAL
5.0 g in 100 g
9/25/2023
McKesson Medical-Surgical
68599-6302
TOPICAL
75 mg in 1 g
1/15/2021

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
ORAL-B SENSITIVE WITH FLUORIDE TOOTHPASTE
oral-b laboratories, a div. of procter & gamble inc
02131552
Toothpaste ,  Cream - Topical
5 %
4/15/1998
SENSODYNE-F MINT TOOTHPASTE
glaxosmithkline consumer healthcare ulc
02232757
Toothpaste - Topical
5 %
5/2/2000
RENITAB
cardinaux-medicinat inc.
02068427
Tablet - Oral
97.2 MG
12/31/1995
SALTPETRE PWR 100%
regal pharms, division of bradcan corporation
00378267
Powder - Oral
100 %
12/31/1978
ALSIDOZ TAB
alsi cie ltee
00393665
Tablet - Oral
97.5 MG
12/31/1977
SALPETRE PWR
lab valmo enregistré, division of technilab inc.
00448214
Powder - Oral
100 %
12/31/1979
SENSITIVE WITH FLUORIDE TPT
oral-b laboratories, a div. of procter & gamble inc
02080397
Toothpaste - Dental
5 %
12/31/1994
KALI NITRICUM GRANULES 5CH-30CH
dolisos laboratoires s.a.
00765902
Tablet - Oral
1 DH / TAB
12/31/1987
LOLLI ASM
terra botanica products ltd.
02233297
Lozenge - Oral
30 C
12/8/1997
SALZMANN PRODUCT M-1 MALENA
biocentre
00696447
Tablet - Oral
3 X / X
12/31/1986

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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