Human Formulations

Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w

Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w is a topical formulation formulated with Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w. The listed active ingredient profile is Potassium Nit

Topical FormulationsOintment & Cream Single Ingredient Topical Formulation
Sterile injectable formulation

Product information

Product Line
Human Formulations
Category
Topical Formulations, Ointment & Cream
Dosage Form
Topical Formulation
Product Type
Single Ingredient

Available strengths

Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w

Description

Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w is a topical formulation formulated with Potassium Nitrate 5% w/w, + Sodium Monofluorophosphate 0.7% + Triclosan 0.5%w/w. The listed active ingredient profile is Potassium Nitrate % w/w; Sodium Monofluorophosphate %; Triclosan w/w, placing the product in the dental / oral care category. The formulation contains oral-care ingredients used for approved dental sensitivity, oral pain, plaque or fluoride-support applications. The dosage form is intended for topical/local application; the exact application site and frequency must follow the approved product instructions. For website cataloguing, the composition, strength, dosage form and formulation characteristics should be displayed prominently and consistently. The product description should remain factual and should not include unapproved cure, superiority, guaranteed-result or broad therapeutic claims. Clinical selection should depend on diagnosis, patient-specific factors, contraindications, concomitant medicines and professional judgement. Prescription status, warnings, interactions, adverse effects and dosing or application instructions must be checked against the current approved product label. Manufacturer, licence, storage, shelf-life, reconstitution where applicable, and market-specific regulatory details should be added only from verified product documentation.
WHO-GMP Sourced
Sterile Supply
Regulatory Documentation
Quality Assured