Alcohol Swabs Suppliers & Bulk Manufacturers
Available Forms: Pre-moistened alcohol swabs, Sterile applicator pads
Available Strengths: Typically contain 70% isopropyl alcohol, available in packs of 50–100 sterile swabs for skin disinfection
Reference Brands: BD (Becton Dickinson), StatSwab, 3M, Medline, EltaMed
Category:
Medical Devices
Alcohol swabs disinfect skin by rapidly killing bacteria, viruses, and fungi through protein denaturation and cell membrane disruption. They provide quick, effective cleaning before injections, blood draws, or wound care, reducing infection risk. Benefits include aseptic procedure assurance, decreased contamination, and enhanced safety in clinical, veterinary, and laboratory settings.
Alcohol swabs is available in Pre-moistened alcohol swabs, Sterile applicator pads
and strengths such as Typically contain 70% isopropyl alcohol, available in packs of 50–100 sterile swabs for skin disinfection.
Sourced from GMP-certified and ISO-compliant manufacturers, this API meets
global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical
formulation and commercial manufacturing, Alcohol swabs is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
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Technical Specifications & Supply Details
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| Lead Time |
7 to 60 days (depending on batch size & schedule) |
| MOQ |
As per manufacturer’s batch size |
| COA |
Available with every batch |
| Regulatory Dossier / DMF |
Available upon request |
| Export Documentation |
FSC, COA, Manufacturing License, Product Permission |
| Standards |
IP, BP, USP |
| Certifications |
WHO-GMP, EU-GMP, USFDA (as applicable) |
Alcohol swabs can be exported to over 30 countries across Asia, Africa, Europe,
and Latin America. Flexible packaging, competitive pricing, and a verified supplier
network make Pharmatradz a trusted sourcing partner for pharmaceutical companies
and contract manufacturers worldwide.
Product Description:
Alcohol swabs are regulated in the EU and US, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP and MDR standards. In the US, FDA approval requires validation, safety testing, and compliance with applicable standards, while in the EU, CE marking certifies conformity with in vitro diagnostic and medical device regulations. These products undergo validation, stability testing, and audits, with comprehensive documentation including safety profiles, performance data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective alcohol swabs for infection control during medical, veterinary, and laboratory procedures worldwide.
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