Products in Nasal

Capmul® GMO-50 glycerol monooleate is a food-grade multifunctional emulsifier that is highly useful in personal care & cosmetic applications such as, lotions, creams, lipsticks, and eyeliners. Capmul GMO-50 is sunflower glycerides and suitable in barrier creams and lotions. It easily forms gel phases with other surfactants in aqueous environments and can serve as a refatting agent. It is an excellent non polymeric invert emulsifier providing an elegant finish to your formulation. It is manufactured in USA.

Capmul® MCM EP/NF is a mixture of monoacylglycerols, obtained by direct esterification of glycerol with caprylic (octanoic) and capric (decanoic) acids. It is manufactured in USA.

Captex® 300 EP/NF is manufactured by the esterification of glycerin and fatty acids, mainly caprylic (‰ˆ70%) and capric. It contains not less than 95% of saturated fatty acids with 8 and 10 carbon atoms. It is prepared from raw materials of vegetable sources. It is miscible with most organic solvents including 96% ethanol. It is manufactured in USA.

Stearoyl macrogolglycerides are mixtures of monoesters, diesters and triesters of glycerol and monoesters and diesters of macrogols (polyethylene glycols (PEG) with a mean relative molecular mass between 300 and 4000). They are obtained by partial alcoholysis of saturated oils containing mainly triglycerides of stearic acid using macrogol (PEG) or by esterification of glycerol and macrogol (PEG) with saturated fatty acids or by mixture of glycerol esters and condensates of ethylene oxide with the fatty acids of these hydrogenated oils. The product may contain free polyethylene glycols, and appears as a pale-yellow, waxy solid. It is manufactured in USA.

Capmul® MCM C8 EP/NF is a mixture of monoacylglycerols, containing variable quantities of diand tri-acylglycerols, obtained by direct esterification of glycerol with caprylic (octanoic) acid. It is manufactured in USA.

Acconon® MC8-2 EP/NF is a mixture of monoesters, diesters, and triesters of glycerol and monoesters and diesters of polyethylene glycols with a mean relative molecular weight between 200-400. It may contain free macrogols. It is manufactured in USA.

Capmul® PG-8 NF is Type II Propylene Glycol Monocaprylate, a propylene glycol monoester of caprylic acid. It is an excellent solvent and a good bioavailability enhancer for many complex, poorly soluble drug compounds. Capmul® PG-8 NF is used primarily as a carrier in soft and hard gelatin capsules and a penetration enhancer in transdermal drug delivery systems. It is manufactured in USA.

Captex® 355 EP/NF/JPE is manufactured by the esterification of glycerin and fatty acids, mainly caprylic (‰ˆ55%) and capric. It contains not less than 95% of saturated fatty acids with 8 and 10 carbon atoms. It is prepared from raw materials of vegetable sources. It is manufactured in USA.

Captex® 355 EP/NF is manufactured by the esterification of glycerin and fatty acids, mainly caprylic (‰ˆ55%) and capric. It contains not less than 95% of saturated fatty acids with 8 and 10 carbon atoms. It is prepared from raw materials of vegetable sources. It is miscible with most organic solvents including 96% ethanol. It is manufactured in USA.

Capmul® PG-12 EP/NF is a propylene glycol monoester of lauric acid. It is an excellent solubilizer for many complex poorly soluble drug compounds. Capmul® PG-12 EP/NF is used primarily as a carrier in soft and hard gelatin capsules, a penetration enhancer in transdermal drug delivery systems, and a secondary emulsifier in microemulsions. It is manufactured in USA.

Oleoyl macrogolglycerides, is a mixture of monoesters, diesters and triesters of glycerol and monoesters and diesters of macrogols (polyethylene glycols (PEG) with a mean relative molecular mass of 300). It is obtained by partial alcoholysis of unsaturated oils containing mainly triglycerides of oleic (cis-9-octadecenoic) acid using macrogol (PEG) or by esterification of glycerol and macrogol (PEG) with unsaturated fatty acids or by mixture of glycerol esters and condensates of ethylene oxide with the fatty acids of these unsaturated oils. The product may contain free polyethylene glycols. It is manufactured in USA.

EXCIPURE™ DPI 222 is a very finely milled cohesive lactose powder which enables the adjustment of fines content when blended with a broad or coarse lactose.

EXCIPURE™ DPI 111 is a coarse sieved lactose carrier with good flow properties which can be blended with micronized or fine lactose.

Niacet’s acetates, mainly sodium acetate are used in the production of insulin. Additionally, as a constituent in insulin products, sodium acetate acts as an oxidative fuel preventing the body from producing antibodies during insulin injection. Sodium Acetate is available as an agglomerate and a powder (anhydrous) as well as a crystal (trihydrate). Sodium Acetate trihydrate is very soluble in water. Sodium Acetate anhydrous agglomerate offers the properties of non-dustiness, improved wettability, higher reactivity, higher bulk density, and improved free-flow ability.

EXCIPURE™ DPI 223 is a finely milled cohesive lactose powder.

EXCIPURE™ DPI 231 is a broad lactose suitable for blister’s devices formulation. It can also be blended with micronized or fine lactose for adjustment of fines content.

Sodium Acetate Trihydrate can be used in pharmaceuticals. Sodium Acetate Trihydrate USP/EP/JP Granulated is a White or colorless granular product.

Sodium Acetate Trihydrate can be used in pharmaceuticals. Sodium Acetate Trihydrate USP/EP Granulated is a White or colorless granulated product.

Unolab Manufacturing 0.9% saline solution and hyaluronic acid is used in a treatment of Nebulisation and inhalation. This Product has a License of MD(lla).

Unolab Manufacturing 3% hypertonic solution with hyaluronic acid is used in a treatment of Nebulisation and inhalation. This Product has a License of MD(lla).

Unolab Manufacturing 7% hypertonic solution with hyaluronic acid is used in a treatment of Nebulisation and inhalation. This Product has a License of MD(lla).

Unolab Manufacturing 1.5% hypertonic solution is used in a treatment of Nebulisation and inhalation. This Product has a License of MD(lla).

Unolab Manufacturing 5% hypertonic solution is used in a treatment of Nebulisation and inhalation. This Product has a License of MD(lla).

Chitin belongs to the biopolymer group and its fibrous structure is similar to cellulose. Chitin is the second most common regenerative polysaccharide after cellulose.

Cyclolab Sulfobutylated beta-cyclodextrin sodium salt (DS~6.5) is an excipient compound incorporating a chemically modified cyclodextrin with a structure that optimizes the solubility and stability of active pharmaceuticals and their properties. It is a highly water-soluble anionic cyclodextrin derivative. It can easily form non-covalent inclusion complexes with drug molecules and therefore reduce drug toxicity and haemolysis as well as control drug release rate. Its complexing properties also make it suitable for masking unpleasant odors and tastes of pharmaceutical products. It is used as an excipient in injection, oral, nasal and eye medication.

Avicel® CL - 611 a non-animal-origin ingredient, is used in sprays and suspensions. It's compatible with various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceuticals, it acts as a binder, filler, stabilizer, and immediate release agent. It's also an emulsifying agent and viscosity modifier, aiding suspension.

Avicel® RC - 591 is versatile, catering to various dosage forms like lotions, sprays, and suspensions. Its manufacturing technology involves direct compression, dry granulation, and wet granulation methods. In pharmaceutical and nutraceutical applications, it serves as a binder, compression aid, immediate release agent, and stabilizer, ensuring product efficacy and stability.