Chlorhexidine Acetate Suppository

Chlorhexidine Acetate Suppository — GMP manufactured suppositories by Artemisine Medicines Technology. Original manufacturer supply with sta

Chlorhexidine Acetate Suppository product packaging
Suppositories

Chlorhexidine Acetate Suppository

Chlorhexidine Acetate Suppository — GMP manufactured suppositories by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product NameChlorhexidine Acetate Suppository
Dosage FormSuppositories
Strength20 mg
StandardsBP / ENTERPRISE
PackingCustomized per market requirement (bottle / blister / box)
DocumentsCOA, COPP, DMF, CTD Dossiers
MOQContact 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▾
WHO essential antiseptic for hand hygiene, skin and wound preparation, surgical scrubbing and umbilical cord care (chlorhexidine); povidone-iodine for skin antisepsis.
💧Administration▾
Apply to intact skin or the affected area and allow to dry; scrub hands for the recommended contact time. For cord care, apply chlorhexidine 7.1% solution once daily for the first week.
⚖️Dosage▾
Use undiluted as supplied for skin antisepsis. For cord care 4% or 7.1% solution applied once daily; do not cover with dressings. Follow local infection-prevention protocols for contact time.
⚠️Precautions & Warnings▾
Do not apply to the eyes, middle ear or mucous membranes (chlorhexidine is ototoxic and neurotoxic if used in the ear canal). Avoid in known allergy; do not mix with other antiseptics. Keep away from infants' faces.

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.

FAQ

Chlorhexidine Acetate Suppository — Frequently Asked Questions

Which documents are provided for Chlorhexidine Acetate Suppository registration?

Every batch of Chlorhexidine Acetate Suppository ships with a Certificate of Analysis (COA). For market registration we provide COPP, DMF and CTD-format dossiers, plus legalisation support where your authority requires it.

What is the MOQ and lead time for Chlorhexidine Acetate Suppository?

MOQ and lead time for Chlorhexidine Acetate Suppository depend on strength, packaging and destination market. Send us your target market and annual volume — our export team confirms current stock, MOQ and lead time within 24 hours.

Do you support OEM / private label?

Yes. We offer OEM packaging and private-label production for Chlorhexidine Acetate Suppository, subject to the regulatory requirements of the destination market.

Which markets have you exported suppositories products to?

We have supplied suppositories products to 50+ countries across Africa, Southeast Asia, Latin America and the Middle East, with experience in ministry-of-health registration and international tenders.

How is the quality of Chlorhexidine Acetate Suppository controlled?

Chlorhexidine Acetate Suppository is produced in China-GMP workshops (site re-inspected and passed in 2026), released only after full QC testing against BP / enterprise standards, with retained samples kept for one year beyond the product's expiry date.

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