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Benzoic acid

Generic Name
Benzoic acid
Brand Names
Ammonul, Hyophen
Drug Type
Small Molecule
Chemical Formula
C7H6O2
CAS Number
65-85-0
Unique Ingredient Identifier
8SKN0B0MIM

Overview

A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. As the sodium salt form, sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids. This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia. Total Positive and Negative Syndrome Scale scores dropped by 21% compared to placebo.

Background

A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. As the sodium salt form, sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids. This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia. Total Positive and Negative Syndrome Scale scores dropped by 21% compared to placebo.

Indication

⑴与水杨酸合用于成龙皮肤真菌病、浅部真菌感染的体癣、手癣及足癣等,但目前有更多的高效抗真菌药,本制剂可作为二线治疗药。也用于食品和药物制剂的防腐剂,一般浓度为0.2%,或用0.5%的苯甲酸钠,溶解度更好。 ⑵用于罕见病精氨酸酶缺乏症的治疗。

Associated Conditions

  • Fungal Infections
  • Oropharyngeal pain
  • Pain
  • Ringworm
  • Sore Throat
  • Tinea Pedis
  • Burning sensation in the mouth
  • Dry cough
  • Oral infections
  • Throat infections

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Mission Pharmacal Company
0178-0745
ORAL
9 mg in 1 1
1/22/2024
Star Pharmaceuticals, LLC
0076-0901
ORAL
9 mg in 1 1
1/5/2017
Showing 2 of 2 FDA approvals

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
TINEA SKIN SOLUTION (THREE LEG BRAND)
SIN08773P
SOLUTION
2% w/v
7/3/1996
VEELANZ'S OINTMENT
SIN16547P
OINTMENT
6.01% w/w
7/7/2022
ROBINSON RINGWORM & WHITESPOT OINTMENT
SIN09544P
OINTMENT
6% w/w
11/21/1997
SAW HONG CHOON SKIN OINTMENT
SIN09830P
OINTMENT
6% w/w
6/18/1998
NIXODERM OINTMENT
SIN04418P
OINTMENT
6.00% w/w
5/3/1990
Showing 5 of 5 HSA approvals

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
NIZO SPRAY
N/A
N/A
N/A
1/29/2001
SUSIK POWDER
N/A
unicorn laboratories o/b american unicorn laboratories limited
N/A
N/A
7/3/1998
DERMACORN FOOT SOAKING POWDER
N/A
unicorn laboratories o/b american unicorn laboratories limited
N/A
N/A
7/14/2011
RADISOL ACID SALICYLIC APPLICATION
N/A
N/A
N/A
1/24/1979
CURCYTOL SKIN LOTION (SPRAY)
N/A
N/A
N/A
2/11/1998
ZEMASALIC OINTMENT
N/A
meyer pharmaceuticals ltd
N/A
N/A
2/16/1994
WHITASALIC OINTMENT
N/A
meyer pharmaceuticals ltd
N/A
N/A
2/16/1994
MAGIC POWDER
N/A
unicorn laboratories o/b american unicorn laboratories limited
N/A
N/A
10/14/2007
ANTIVE SKIN LOTION
N/A
N/A
N/A
9/19/1981
RICH POWDER
N/A
unicorn laboratories o/b american unicorn laboratories limited
N/A
N/A
9/29/1999
Showing 10 of 20 PPB approvals
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