Human Formulations

Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/

Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/ is a topical formulation formulated with Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/. The listed active ingredient profile is Clindam

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

Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/

Description

Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/ is a topical formulation formulated with Clindamycin Phosphate 1.00%w/w Sodium Methyparaban0.1%w/w Phenoxyehenol 0.25% w/w/. The listed active ingredient profile is Clindamycin Phosphate w/w Sodium Methyparaban0. w/w Phenoxyehenol % w/w, placing the product in the topical antibacterial / dermatology category. The formulation contains topical antibacterial ingredient(s) intended for susceptible localized bacterial skin conditions. 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