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White Vaseline BP EP USP Pharma Grade comes straight from refined, purified petroleum jelly. In my experience working in product manufacturing, it’s a staple for its clean, inert composition. No scents, no added color—just a uniform white, translucent material that blends into pharmaceutical, cosmetic, and personal care formulas. Users value it for its consistency and gentle character. I’ve seen it function as a base in moisturizing balms and topical ointments. Lab teams depend on clear benchmarks: this grade lines up with British Pharmacopoeia (BP), European Pharmacopoeia (EP), and United States Pharmacopeia (USP) standards. These standards confirm the product stays free from contaminants, making sure it won’t introduce foreign substances into sensitive applications.
From a chemical standpoint, White Vaseline relies on a mix of semi-solid hydrocarbons. Its backbone includes saturated hydrocarbons with Carbon and Hydrogen atoms forming a long, unbranched chain. The empirical molecular formula reflects a hydrocarbon composition, which roughly translates to (CnH2n+2), where ‘n’ varies, accounting for the blend of chain lengths. This precise formulation ensures reliable, reproducible performance each time it’s sourced. As a material, it appears as a smooth, white and translucent solid at room temperature, yet softens quickly with a little heat. You can scoop, spread, or mold it without much effort—a property many in pharma and cosmetics appreciate.
Every specification tells a story about safety, purity, and reliability. White Vaseline BP EP USP Pharma Grade generally holds a melting point in the range of 50-60°C. Its specific gravity (density compared to water) sits between 0.820 and 0.885 at 25°C. Pure to the eye, odorless, and tasteless, it keeps contaminants like acid, alkali, or unsaponifiable matter below demanding pharmacopeial limits. This grade resists oxidation and chemical change, holding firm under most storage conditions. Whether delivered as blocks, flakes, pearls, or solid slabs, the texture remains soft and easily workable—never gritty or crystalline. If someone prefers a more liquid consistency, light heating turns it into a pourable solution. Its density lets it float on water, deliver a protective barrier on skin, and serve as a stable base for sensitive pharma compounds.
Storage and delivery require clean, airtight containers to prevent contamination. I’ve watched factories package White Vaseline in drums, pails, or lined cartons, ensuring transport safety by sealing against dust and humidity. The HS Code for international trade usually reads as 2712.10, covering petroleum jelly and other waxy substances. This code guides customs declarations and traceability through global supply chains. From my experience, tracking with the HS Code speeds up inspections, reduces clearance issues, and reassures clients about consistency batch to batch.
Every batch of White Vaseline BP EP USP Pharma Grade comes with documents detailing its safety and handling requirements. Classified as non-hazardous for routine use under most regulatory systems, this substance still deserves respect in the workplace. Protective clothing, proper ventilation, and strict hygiene practices guard against cross-contamination—a lesson I learned early while supervising a compounding room. Accidental ingestion, inhalation, or contact won’t cause harm in standard use because the jelly doesn’t contain reactive chemicals, solvents, or volatile components. Disposal routines recommend recycling unused or expired Vaseline in line with local waste protocols. Warehouses pay close attention to temperature—excessive heat softens or melts the material, though freezing does little to alter texture or safety. Sheets like the Safety Data Sheet (SDS) always clarify that the jelly won’t support microbial growth, preventing risks of cross-infection in clinical and skincare settings.
Everything starts with crude petroleum, refined to exacting standards through distillation and purification. My time liaising with quality teams has shown that only high-purity hydrocarbons make it through, with every step monitored for sulphur, nitrogen, and aromatic residue. Any hint of contamination gets flagged, stopping the batch from continuing toward pharma-grade status. The refining process transforms raw oil into a clear, uniform jelly free from offensive smell, taste, or color. Raw materials shape the material’s smooth structure and the even melting experience valued by end users.
White Vaseline BP EP USP Pharma Grade shows up in ointments for skin care, lip treatments, wound protection, and as a lubricating base in medical device manufacturing. I often see cosmetic firms reach for it in cream and lotion formulas because the final product always delivers gentle, predictable texture and spreadability. Medical-grade Vaseline plays a key role as an occlusive—trapping moisture, stopping scab lifting, and keeping wounds in a healthy environment for healing. Its inert quality fits right into dental pastes, adhesive removers, and baby skincare solutions. For every innovation—whether that’s enhanced medicated ointments or specialty creams—manufacturers trust pharma-grade Vaseline to carry active ingredients without breaking down or causing allergic responses.
Earning a label like BP, EP, or USP means something. Auditors visit production lines, review process controls, and verify records. I’ve seen manufacturers undergo repeated quality checks, from raw material acceptance through to product release testing. The documentation and batch records trail goes deep, tightening controls and keeping track of every stage. Clients who request premium grades count on this assurance—after all, pharma-grade Vaseline often sits next to sensitive active drugs, newborn care products, or post-operative dressings. Any slip in quality risks more than recalls—it can reach the level of patient safety, so there’s no room for compromise.
The industry faces pressure to trace sources for each batch, reduce contaminants even further, and prove sustainability at every turn. Keeping up with new regulatory rules about hydrocarbons pushes manufacturers to invest in better refining and more rigorous documentation. Others weigh the benefits of biodegradable or plant-derived alternatives for clients who want greener options. Facilities that lean into automation and digitized record-keeping prevent mistakes in manufacturing and reduce the risk of human error. Every time I’ve worked with teams to implement traceability, quick access to batch histories made recalls and audits possible without chaos.
The steady popularity of White Vaseline BP EP USP Pharma Grade traces back to everyday, dependable properties. It’s more than a neutral raw material. This jelly builds trust, proves its performance across product lines, and will keep its place in pharma, personal care, and medical manufacturing as long as the industry values purity, safety, and lasting quality. Solutions for the future tie back to cleaner sourcing, tighter control systems, and a focus on user safety—from lab to warehouse to final customer.
Chengguan District, Lanzhou, Gansu, China
