Name: Neomycin Sulfate Eye Drops
Brand: Artemisine Medicines Technology Co., Ltd.

Ophthalmic

Neomycin Sulfate Eye Drops

Neomycin Sulfate Eye Drops — GMP manufactured ophthalmic by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Neomycin Sulfate Eye Drops
Dosage Form	Ophthalmic
Strength	40000 IU/mL
Standards	BP / ENTERPRISE
Packing	Customized per market requirement (bottle / blister / box)
Documents	COA, COPP, DMF, CTD Dossiers
MOQ	Contact us for MOQ and current stock

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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾

Bacterial blepharitis, conjunctivitis, keratitis and corneal ulcer caused by susceptible Gram-negative and Gram-positive organisms.

💧Administration▾

Topical ocular instillation into the conjunctival sac; apply ointment by pulling the lower lid and squeezing a 1 cm strip inside, avoiding contact with the eye.

⚖️Dosage▾

1–2 drops every 4 hours (severe infection every hour initially, reducing as it improves); ointment 2–3 times daily; usually no longer than 7–10 days.

⚠️Precautions & Warnings▾

Prolonged use may lead to fungal or resistant bacterial overgrowth and, rarely, local irritation. For ophthalmic use only; aminoglycoside eye drops should not be used long term in patients with corneal epithelial defects.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

Why Order From Us

Factory Direct. Fully Documented.

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GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

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Fast Delivery

Sufficient stock on regular items, familiar with export logistics to 50+ countries.

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Registration Support

COA, DMF, dossier and legalization documents for your market registration.