Human Formulations

Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w Ointment

Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w Ointment is a ointment formulated with Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w. The listed active ingre

Topical FormulationsOintment & Cream Single Ingredient Ointment
Sterile injectable formulation

Product information

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

Available strengths

Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w

Description

Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w Ointment is a ointment formulated with Povidone-Iodine IP 5%w/w + (Availabe lodine 0.5%w/w) Metronidazole P 1%w/w + Aloe Vera 1.595w/w. The listed active ingredient profile is Povidone-Iodine w/w; Metronidazole P w/w; Aloe Vera, placing the product in the antiseptic / wound care category. The formulation contains antiseptic and/or wound-care ingredients intended for selected topical wound or skin-care 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