IP Library Granted Patent US 7,115,273
Granted Patent B2
US 7,115,273 · App. 09/753,136 · Granted Oct 3, 2006

Anti-viral lotion tissue, and methods for making and using the same

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Quick Facts
Patent No.
US 7,115,273
App. No.
09/753,136
Granted
Oct 3, 2006
Kind
B2
Abstract

A soothing anti-viral lotion composition and a lotioned tissue product having a surface with the lotion composition applied thereto, and methods for making and using the same. The lotion composition includes an anti-viral organic acid and a topical delivery system. The topical delivery system includes one or more polyesters which allow incorporation of the organic acids into the lotion formulation, controls their delivery, and maintains them in the stratum corneum. The lotion composition may optionally contain a surfactant, an irritation inhibiting agent, and other additives.

Claims (24)

1. A non-irritating anti-viral lotioned tissue product having applied to at least one surface thereof an anti-viral lotion composition comprising:

about 1% to about 25% of at least one anti-viral organic acid, said anti-viral organic acid comprising carboxylic acid having the structure R-COOH, wherein R is C 1 –C 6 alkyl carboxyhydroxy;

about 5% to about 25% of an emollient including at least one polyester, said polyester comprising trimethylpentanediol/adipic isononanoic acid copolymer; and

a cationic surfactant.

2. A lotioned tissue product having applied to at least one surface thereof an anti-viral lotion composition comprising:

about 1% to about 25% of at least one anti-viral organic acid, said anti-viral organic acid comprising carboxylic acid having the structure R-COOH, wherein R is C 1 –C 6 alkyl carboxyhydroxy;

about 5% to about 25% of an emollient including at least one polyester, said polyester comprising trimethylpentanediol/adipic acid copolymer; and

a cationic surfactant.

3. The lotioned tissue product of claim 2 , wherein said cationic surfactant comprises a quaternary ammonium compound.

4. A non-irritating, anti-viral lotion composition comprising:

about 1% to about 25% of at least one anti-viral organic acid, said anti-viral organic acid comprising carboxylic acid having the structure R-COOH, wherein R is C 1 –C 6 alkyl carboxyhydroxy;

about 5% to about 25% of an emollient including at least one polyester, said polyester comprising trimethylpentanediol/adipic isononanoic acid copolymer; and

a cationic surfactant.

5. A anti-viral lotion composition comprising:

about 1% to about 25% of at least one anti-viral organic acid, said anti-viral organic acid comprising carboxylic acid having the structure R-COOH, wherein R is C 1 –C 4 alkyl carboxyhydroxy;

about 5% to about 25% of an emollient including at least one polyester, said polyester comprising trimethylpentanediol/adipic acid copolymer; and

a cationic surfactant.

6. The lotion composition of claim 5 , wherein said cationic surfactant comprises a quaternary ammonium compound.

7. A method of inhibiting the transfer of a viral infection comprising:

providing anti-viral lotion tissue product having applied to at least one surface thereof an anti-viral lotion composition comprising about 1% to about 25% of at least one anti-viral organic acid, said anti-viral organic acid comprising carboxylic acid having the structure R-COOH, wherein R is C 1 –C 6 alkyl carboxyhydroxy, about 5% to about 25% of an emollient including at least one polyester, said polyester comprising trimethylpentanediol/adipic acid copolymer, and a cationic surfactant;

contacting a fluid containing at least one virus with said anti-viral tissue product; and

absorbing said fluid within said absorbent article to contact the fluid with said anti-viral lotion composition.

8. The method of claim 7 , further comprising:

transferring a portion of the lotion composition to the user of the tissue product.

Assignments (1)
NAME CHANGE Recorded Feb 3, 2015
From: KIMBERLY-CLARK WORLDWIDE, INC.
To: KIMBERLY-CLARK WORLDWIDE, INC.
Reel/Frame 034880/0742 →