IP Library Patent Application 13389775
Patent Application
App. No. 13/389,775

PHARMACEUTICAL SOLUTION OF CETIRIZINE HYDROCHLORIDE

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Quick Facts
Patent No.
US None
App. No.
13/389,775
Abstract

A pharmaceutical solution comprising cetirizine hydrochloride, an alcohol compound with less than 3 carbon atoms, a preservative and urea is disclosed. The cetirizine hydrochloride is in racemic form or in levo form.

Claims (140)

1 . A pharmaceutical solution of cetirizine hydrochloride, characterized by comprising the following components:

Cetirizine hydrochloride

0.1~2

parts by weight;

Alcohol having 3 or less carbon atoms

1-50

parts by weight;

Preservative

0.01~0.2

parts by weight;

Urea

0.02~20

parts by weight; and

Inorganic salt

0~5

parts by weight,

Wherein said cetirizine hydrochloride is racemic cetirizine hydrochloride or L-cetirizine hydrochloride.

2 . The pharmaceutical solution according to claim 1 , characterized by comprising the following components:

Cetirizine hydrochloride

0.2~2

parts by weight;

Alcohol having 3 or less carbon atoms

10-40

parts by weight;

Preservative

0.01~0.2

parts by weight;

Urea

1~5

parts by weight; and

Inorganic salt

0~5

parts by weight,

Wherein said cetirizine hydrochloride is L-cetirizine hydrochloride.

3 . The pharmaceutical solution according to claim 2 , characterized by comprising the following components:

L-cetirizine hydrochloride

0.5~1.5

parts by weight;

Alcohol having 3 or less carbon atoms

15-40

parts by weight;

Preservative

0.05~0.2

parts by weight;

Urea

1~3

parts by weight; and

Inorganic salt

0~5

parts by weight.

4 . The pharmaceutical solution according to claim 3 , characterized by comprising the following components:

L-cetirizine hydrochloride

1

part by weight;

Alcohol having 3 or less carbon atoms

15-40

parts by weight;

Preservative

0.1

parts by weight;

Urea

2

parts by weight; and

Inorganic salt

0.5~1.5

parts by weight.

5 . The pharmaceutical solution according to claim 1 , characterized in that said alcohol having 3 or less carbon atoms is propanediol, glycerin, propanol, ethanol or any combination thereof; said preservative is one or two selected from benzalkonium bromide, chlorhexidine acetate, sodium benzoate and sorbic acid; and said inorganic salt is one or more selected from sodium chloride, potassium chloride, sodium sulfate, potassium sulfate, calcium chloride and sodium bicarbonate.

6 . The pharmaceutical solution according to claim 5 , characterized in that said alcohol having 3 or less carbon atoms is glycerin or 1,2-propanediol; said preservative is benzalkonium bromide or chlorhexidine acetate; and said inorganic salt is sodium chloride.

7 . The pharmaceutical solution according to claim 6 , characterized in that said alcohol having 3 or less carbon atoms is glycerin and said preservative is benzalkonium bromide.

8 . The pharmaceutical solution according to claim 1 , characterized in that the pH of the pharmaceutical solution is 5.0˜7.0.

9 . The pharmaceutical solution according to claim 8 , characterized in that the pH of the pharmaceutical solution is 6.0.

10 . The pharmaceutical solution according to claim 1 , characterized in that said pharmaceutical solution is liniment, drops, aerosol or spray.

11 . The pharmaceutical solution according to claim 5 , characterized in that said pharmaceutical solution further comprises a flavoring agent which is orange peel oil, anise oil, citron oil, citron tincture, a fragrant, cinnamon water, cinnamon oil, banana essence, orange essence, lemon essence or apple essence.

12 . The pharmaceutical solution according to claim 1 , characterized by comprising the following components:

Cetirizine hydrochloride

0.1~2

parts by weight;

Alcohol having 3 or less carbon atoms

1-50

parts by weight;

Preservative

0.02~0.2

parts by weight;

Urea

0.02~20

parts by weight; and

Inorganic salt

0.01~2

parts by weight,

wherein said cetirizine hydrochloride is racemic cetirizine hydrochloride, said alcohol having 3 or less carbon atoms is glycerin; said preservative is benzalkonium bromide; and said inorganic salt is sodium chloride.

13 . The pharmaceutical solution according to claim 12 , characterized by comprising the following components:

Cetirizine hydrochloride

0.5~1.5

parts by weight;

Glycerin

5-40

parts by weight;

Urea

1~6

parts by weight;

Benzalkonium bromide

0.02~0.15

parts by weight; and

Sodium chloride

0.5~1.5

parts by weight.

14 . The pharmaceutical solution according to claim 13 , characterized by comprising the following components:

Cetirizine hydrochloride

1

part by weight;

Glycerin

35-40

parts by weight;

Urea

1~3

parts by weight;

Benzalkonium bromide

0.08~0.12

parts by weight; and

Sodium chloride

0.5~1.5

parts by weight.

15 . The pharmaceutical solution according to claim 14 , characterized by comprising the following components:

Cetirizine hydrochloride

1

part by weight;

Glycerin

37.8

parts by weight;

Urea

2

parts by weight;

Benzalkonium bromide

0.1

parts by weight; and

Sodium chloride

0.9

parts by weight.

16 . The pharmaceutical solution according to claim 12 , characterized in that the pH of the pharmaceutical solution is 4.0˜7.5.

17 . The pharmaceutical solution according to claim 16 , characterized in that the pH is 5.0˜7.0.

Assignments (3)
TERMINATION AND RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY RECORDED AT REEL 52252, FRAME 0289 Recorded Mar 30, 2026
From: GALLAGHER IP SOLUTIONS LLC, AS SUCCESSOR TO NEWLIGHT CAPITAL, LLC; UMB BANK, NATIONAL ASSOCIATION
To: TIGO ENERGY, INC.
Reel/Frame 075311/0457 →
SECURITY INTEREST Recorded Mar 27, 2020
From: TIGO ENERGY, INC.
To: NEWLIGHT CAPITAL, LLC; UMB BANK, NATIONAL ASSOCIATION, AS TRUSTEE
Reel/Frame 052252/0289 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2012
From: ZHAO, ZHIQUAN
To: LUNAN BETTER PHARMACEUTICAL CO., LTD.
Reel/Frame 027681/0630 →