Liposomal Glutathione Supplement Manufacturer | Private Label & OEM

These are commercially established starting points for a finished liposomal glutathione SKU, including private-label launches. Pick the closest concept or send your current formula. KS formulation team and R&D center match channel and destination market, then confirm GSH milligrams, the phospholipid file, and whether encapsulation efficiency is on release. You receive a SKU-level cost, a feasibility read, and a sample plan. Label claims remain the brand’s responsibility.

If the brief is an antioxidant assortment of several SKUs, start from antioxidant supplements and treat liposomal GSH as one architecture on that line.

Milligram bands below are development examples.

A dry glutathione drum COA does not prove a liposomal finished unit. Name these fields before comparing suppliers.

Declared strength. Count milligrams as reduced GSH in the finished piece (or as mg/mL × serving mL on a liquid). S-acetyl is a different labeled ingredient and a different quote — not a 1:1 swap onto this milligram line.

Phospholipid system. Sunflower versus soy, phosphatidylcholine percentage, and allergen status belong on the raw-material file. A marketing “liposomal blend” name is not a substitute for that identity.

Encapsulation efficiency. If the artwork will print liposomal, name the EE method and whether EE is a release field. Without a method, do not print liposomal. Incoming premix paperwork from a third party is not automatically the vesicle file for your finished batch.

Particle size. A size range can sit on the project file as a conversation. It is not a site-wide guarantee. Drift after homogenization, fill, or freight is a stability question for that pack and climate.

GSH assay and GSH/GSSG. Release named glutathione content with a named method (HPLC is the usual commercial conversation). In liquids, sticks, and gummies, GSH/GSSG belongs on release more often than on a dry capsule, because the thiol sits in water or sees heat. GSSG is a ratio or oxidation check — not a second labeled glutathione SKU.

Overage. Overage follows stability data for that matrix and pack. It is not a license to skip barrier, headspace, or finished-unit assay.

Finished-unit testing. Assay of finished liquids, capsules, sticks, or gummies in addition to the incoming drum. Metals and microbiology follow the SKU file, same gate as other oral dietary supplements.

Packaging. Name pack with climate, not as a generic bottle line.

• Temperate markets or short distribution: A light-protected bottle plus scoped headspace or nitrogen is a common starting pack for liposomal liquids.
• Humid markets or long ocean freight: A higher-barrier bottle (or equivalent laminate on sticks) is discussed more often than a standard bottle alone. Do not quote “HDPE 60 count” as the whole pack story.
• Nitrogen / headspace: a process option scoped with pack and climate — not a universal line setting.

When two sources disagree, send both documents against the same declared strength, the same method names, and — if the label says liposomal — the same EE method.

Samples typically run 7–15 days after the formulation is approved. Pilot runs often start near 500–1,000 finished units while the vesicle file and pack are still moving. Capsule programs typically start near 5,000 finished units; a standard lot is commonly 4–6 weeks after formula, artwork, and testing are agreed. Softgels, stick packs, and gummies are often quoted from about 10,000, by die, film, or cook. Re-orders on an approved file are shorter than a first commercial run.