A61Q19/10

Personal care compositions comprising zinc : usnic acid complexes and methods of use

Disclosed herein are personal care compositions comprising Zn:usnate complexes having a 1:2 zinc to usnate molar ratio. Methods of making and using the compositions are also provided. The personal care compositions may include a cleansing component and an antibacterial component, wherein the antibacterial component comprises Zn:usnate complexes having a 1:2 zinc to usnate molar ratio.

Personal care compositions comprising zinc : usnic acid complexes and methods of use

Disclosed herein are personal care compositions comprising Zn:usnate complexes having a 1:2 zinc to usnate molar ratio. Methods of making and using the compositions are also provided. The personal care compositions may include a cleansing component and an antibacterial component, wherein the antibacterial component comprises Zn:usnate complexes having a 1:2 zinc to usnate molar ratio.

Hand sanitizer and method of making the same

The hand sanitizer may be a hand foam sanitizer or a hand gel sanitizer. Each of the hand sanitizers includes at least one stabilizing agent, at least one skin care agent, and a volume of disinfecting micelle capsules suspended therein. Each disinfecting capsule has a polymer shell which defines a hollow core. The polymer shell includes an antimicrobial material. The antimicrobial material may have a concentration of between 0.5 wt % and 95 wt % of the polymer shell. In order to make the hand foam sanitizer, at least one foaming agent is added to produce a foam by air foaming. The hollow core of each disinfecting capsule may be filled with a material, such as at least one disinfectant, at least one fragrance, at least one supplemental skin care agent, or combinations thereof.

Hand sanitizer and method of making the same

The hand sanitizer may be a hand foam sanitizer or a hand gel sanitizer. Each of the hand sanitizers includes at least one stabilizing agent, at least one skin care agent, and a volume of disinfecting micelle capsules suspended therein. Each disinfecting capsule has a polymer shell which defines a hollow core. The polymer shell includes an antimicrobial material. The antimicrobial material may have a concentration of between 0.5 wt % and 95 wt % of the polymer shell. In order to make the hand foam sanitizer, at least one foaming agent is added to produce a foam by air foaming. The hollow core of each disinfecting capsule may be filled with a material, such as at least one disinfectant, at least one fragrance, at least one supplemental skin care agent, or combinations thereof.

FLUSHABLE WIPE AND METHOD OF FORMING THE SAME

A single or multi-ply flushable and dispersible wet wipe including a wet laid fibrous web imprinted using a structuring fabric, a binder composition comprising poly(vinyl) alcohol, poly(vinyl) acetate, poly (ethylene) (vinyl) alcohols, poly (ethylene) (vinyl) acetate, copolymers of vinyl acetate-ethylene, or combinations thereof, and one or more additives. In an exemplary embodiment, the fibrous web is wetted by a wetting solution comprising 0.1% to about 10% by weight of one of the following: (1) boric acid; and (2) boric acid and a mono or divalent salt.

FLUSHABLE WIPE AND METHOD OF FORMING THE SAME

A single or multi-ply flushable and dispersible wet wipe including a wet laid fibrous web imprinted using a structuring fabric, a binder composition comprising poly(vinyl) alcohol, poly(vinyl) acetate, poly (ethylene) (vinyl) alcohols, poly (ethylene) (vinyl) acetate, copolymers of vinyl acetate-ethylene, or combinations thereof, and one or more additives. In an exemplary embodiment, the fibrous web is wetted by a wetting solution comprising 0.1% to about 10% by weight of one of the following: (1) boric acid; and (2) boric acid and a mono or divalent salt.

METHOD FOR DETERMINING RINSE PROPERTIES

A method of measuring rinse properties of a composition from a surface, the method includes providing a cosmetic treatment composition. The method also includes applying the cosmetic treatment composition to a surface. The method also includes rinsing the surface with a first amount of water after applying the cosmetic treatment composition to the surface. The method also includes collecting a portion of the first amount of water after rinsing the surface with the first amount of water. The method also includes measuring a first turbidity of the portion of the first amount of water after collecting the portion of the first amount of water.

ANHYDROUS COMPOSITION FOR TOPICAL USE THAT IS IN THE FORM OF A DISPERSED PHASE BASED ON AT LEAST ONE SHORT DIOL IN A CONTINUOUS FATTY PHASE
20220378672 · 2022-12-01 ·

Composition for topical use including a gelled phase dispersed in a continuous phase, with: the gelled phase including a diol having 3-8 atoms and represented either by formula (Ia): R.sup.a1-C(R.sup.b1)(OH)—C(OH)(R.sup.c1)(R.sup.d1) (Ia), in which each of the Ra1, Rb1, Rc1 and Rd1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, or by formula (Ib): R.sup.a1-C(R.sup.b1)(OH)—[C(R.sup.e1)(R.sup.f1)]t-C(OH)(R.sup.c1)(R.sup.d1) (Ib), in which t is equal to one, two or three, each of the R.sup.a1, R.sup.b1, R.sup.c1, R.sup.d1, R.sup.e1 and R.sup.f1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, it being understood that at least one of the Ra1 or Rb1 radicals and/or at least one of the Rc1 or Rd1 radicals do not represent a hydrogen atom, and —a fatty phase including an oil, an emulsifying surfactant system and an emulsifying surfactant.

ANHYDROUS COMPOSITION FOR TOPICAL USE THAT IS IN THE FORM OF A DISPERSED PHASE BASED ON AT LEAST ONE SHORT DIOL IN A CONTINUOUS FATTY PHASE
20220378672 · 2022-12-01 ·

Composition for topical use including a gelled phase dispersed in a continuous phase, with: the gelled phase including a diol having 3-8 atoms and represented either by formula (Ia): R.sup.a1-C(R.sup.b1)(OH)—C(OH)(R.sup.c1)(R.sup.d1) (Ia), in which each of the Ra1, Rb1, Rc1 and Rd1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, or by formula (Ib): R.sup.a1-C(R.sup.b1)(OH)—[C(R.sup.e1)(R.sup.f1)]t-C(OH)(R.sup.c1)(R.sup.d1) (Ib), in which t is equal to one, two or three, each of the R.sup.a1, R.sup.b1, R.sup.c1, R.sup.d1, R.sup.e1 and R.sup.f1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, it being understood that at least one of the Ra1 or Rb1 radicals and/or at least one of the Rc1 or Rd1 radicals do not represent a hydrogen atom, and —a fatty phase including an oil, an emulsifying surfactant system and an emulsifying surfactant.

ANHYDROUS COMPOSITION FOR TOPICAL USE THAT IS IN THE FORM OF A DISPERSED PHASE BASED ON AT LEAST ONE SHORT DIOL IN A CONTINUOUS FATTY PHASE
20220378672 · 2022-12-01 ·

Composition for topical use including a gelled phase dispersed in a continuous phase, with: the gelled phase including a diol having 3-8 atoms and represented either by formula (Ia): R.sup.a1-C(R.sup.b1)(OH)—C(OH)(R.sup.c1)(R.sup.d1) (Ia), in which each of the Ra1, Rb1, Rc1 and Rd1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, or by formula (Ib): R.sup.a1-C(R.sup.b1)(OH)—[C(R.sup.e1)(R.sup.f1)]t-C(OH)(R.sup.c1)(R.sup.d1) (Ib), in which t is equal to one, two or three, each of the R.sup.a1, R.sup.b1, R.sup.c1, R.sup.d1, R.sup.e1 and R.sup.f1 radicals represent, independently of one another, a hydrogen atom or saturated aliphatic radical having 1-5 carbon atoms, it being understood that at least one of the Ra1 or Rb1 radicals and/or at least one of the Rc1 or Rd1 radicals do not represent a hydrogen atom, and —a fatty phase including an oil, an emulsifying surfactant system and an emulsifying surfactant.