U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-.

Cover of StatPearls

StatPearls [Internet].

Show details

Bacitracin Topical

; ; ; ; .

Author Information and Affiliations

Last Update: June 8, 2024.

Continuing Education Activity

This educational initiative on topical bacitracin offers healthcare practitioners essential insights and resources for effectively utilizing this antibiotic in treating minor skin injuries such as cuts, scrapes, and burns. Bacitracin is a staple in professional settings and home first aid kits, available as a single-agent ointment and in a triple-therapy combination with neomycin and polymyxin B. The program outlines indications, mechanisms of action, safe administration practices, adverse effects, and contraindications, emphasizing proper patient education on the application and duration of treatment to optimize outcomes. Key elements of this initiative include the emphasis on monitoring patients for signs of allergic reactions and educating healthcare providers on making informed decisions to minimize adverse effects. This educational activity seeks to enhance healthcare providers' capabilities in managing infections effectively treated with topical bacitracin, ultimately aiming to improve patient outcomes.

Objectives:

  • Identify the indications for topical bacitracin.
  • Evaluate the antimicrobial mechanism of action of bacitracin.
  • Assess the potential adverse drug reactions of topically-applied bacitracin.
  • Communicate effective collaboration strategies among interprofessional team members to improve outcomes and treatment efficacy for patients who might benefit from bacitracin topical therapy.
Access free multiple choice questions on this topic.

Indications

Bacitracin, a topical antibiotic ointment, is commonly used by medical professionals and the general public to treat minor skin injuries such as cuts, scrapes, and burns. The discovery of bacitracin dates back to 1945, stemming from the wound of a 7-year-old American girl named Margaret Tracey. The debris collected from her leg injury cultured several related cyclic polypeptides produced by a member of the Bacillus subtilis group, which led to the naming of the antibiotic.[1]

United States Food and Drug Administration (FDA)-Approved Indications

FDA approved bacitracin in 1948 to prevent and treat acute and chronic localized skin infections. Bacitracin can be administered less frequently as an intramuscular injection to treat infantile streptococcal pneumonia and empyema. Bacitracin is available as a single-agent ointment or combined with neomycin and polymyxin B into a triple-therapy ointment. The latter is available over the counter at local pharmacies.[2] Additionally, the FDA has approved ocular bacitracin for treating superficial infections of the cornea and conjunctiva caused by susceptible organisms.

Off-Label Uses

The American Academy of Ophthalmology recommends using bacitracin for Pediculosis palpebrarum caused by Phthirus pubis. Forceps can remove adult lice and nits from the eyelids and eyelashes. If nits are firmly attached, the affected lashes may need to be epilated. A mild ophthalmic ointment such as bacitracin or erythromycin should be applied 2 to 3 times daily over 10 days to remove adult lice and nits completely.[3] In a randomized controlled trial, researchers evaluated the effectiveness of various topical agents against Propionibacterium acnes. The results indicated that a triple antibiotic ointment containing neomycin, bacitracin, and polymyxin B effectively inhibited bacterial growth.[4] The Infectious Diseases Society of America guidelines suggest oral bacitracin may be considered for treating initial Clostridium difficile infections. However, alternative medications are preferred due to inadequate evidence and concerns about antimicrobial resistance.[5]

Mechanism of Action

Bacitracin is a mixture of several closely related cyclic polypeptide antibiotics that exhibit both bacteriostatic and bactericidal properties, depending on the drug's concentration and the microorganism's susceptibility. It is effective against many gram-positive bacteria, including species of Staphylococcus, Streptococcus, Corynebacterium, Clostridium, and Actinomyces. Some gram-negative organisms, such as species of Neisseria, are also susceptible to bacitracin; however, most gram-negative organisms are resistant.[6][7] Bacitracin is readily absorbed through denuded, burned, or granulated skin, functioning to inhibit the transfer of mucopeptides into the cell walls of various microorganisms. This action blocks bacterial cell wall synthesis and, ultimately, bacterial replication. Additionally, bacitracin inhibits proteases and other enzymes that alter bacterial cell membrane function. Specifically, it inhibits bacterial cell wall synthesis by preventing the dephosphorylation of the P-P-phospholipid carrier, which attaches the cell wall peptidoglycan precursor units to the cell membrane, resulting in bacterial cell lysis.[8] The stability of bacitracin is enhanced when complexed with zinc.[9]

Pharmacokinetics 

Absorption: Bacitracin is poorly absorbed systemically when applied in topical, ophthalmic, and oral formulations but achieves quick and complete absorption when administered intramuscularly. However, topical bacitracin can be absorbed through burned, denuded skin or areas with granulating tissue.

Distribution: Bacitracin is widely distributed throughout the body, reaching all major organs. Following intramuscular injection, it is present in ascitic and pleural fluids. Bacitracin exhibits minimal protein binding.

Metabolism: Bacitracin is primarily metabolized into smaller peptides and amino acids. The primary metabolite, des-amido-bacitracin, is microbiologically inactive. Additionally, catabolic peptides are formed during the metabolism process.

Excretion: Bacitracin is primarily excreted through the kidneys, with about 87% of an intramuscular dose eliminated through urine within 6 hours. Hydrolytic cleavage products, including di- and tripeptides, are found in urine and bile.

Administration

Available Dosage Forms and Strength

In the USA, bacitracin is available in topical and ophthalmic forms. The topical formulation is an ointment with a concentration of 500 units/g.

Adult Dosage

Topical: Bacitracin is primarily employed as a topical agent, applied directly to wounds or infected areas. Additionally, this antibiotic is available as an ophthalmic ointment formulated explicitly for treating superficial infections of the conjunctiva and cornea.[10]

Before application, the skin should be cleaned gently using mild soap and water. After cleansing, sufficient ointment must be applied to cover the affected areas. Covering the wound with a sterile dressing may aid the healing process and prevent further contamination of the wound site.

Ophthalmic formulation: Bacitracin ointment should be applied directly into the conjunctival sac 1 to 3 times daily. All scales and crusts must be removed in blepharitis cases, followed by a uniform ointment application over the lid margins. When applying the ointment directly to the infected eye, patients are advised to take appropriate precautions to prevent contamination.

Specific Patient Populations

Hepatic impairment: Edit this: Manufacturers do not provide any information regarding the dosage adjustment for bacitracin. Therefore, this medication should be used with caution.

Renal impairment: The parenteral formulations of bacitracin can cause nephrotoxicity and should be used with caution.

Pregnancy considerations: Topical bacitracin, previously classified as FDA pregnancy risk category C, has not been extensively studied for use during pregnancy or lactation. Current evidence does not indicate an increased risk of adverse fetal development. However, due to limited data, caution is advised. Healthcare providers should carefully weigh the risks versus benefits and consider alternative treatments when feasible to ensure the safety of both mother and infant. Further research is necessary to fully understand the safety profile of topical bacitracin during pregnancy and breastfeeding.[11]

Breastfeeding considerations: Topical and ophthalmic formulations of bacitracin generally exhibit minimal absorption through the skin, posing a low risk to nursing infants. Using water-soluble creams or gel products exclusively on breast tissue is recommended to reduce potential exposure from licking.[12]

Edit this: Topical and ophthalmic formulations of bacitracin generally exhibit minimal absorption through the skin, presenting a low risk to nursing infants. To mitigate potential exposure to mineral paraffin from licking, it is recommended that water-soluble creams or gel products be used exclusively on breast tissue.[12]

Pediatric patients: Bacitracin has received FDA approval for treating blepharitis and superficial infections affecting the conjunctiva or cornea.

Older patients: See adult dosage and administration.

Adverse Effects

When used topically as a single agent ointment or part of a triple therapy ointment, bacitracin, and its drug formulation components may cause allergic contact dermatitis. Additionally, cases involving anaphylactic reactions to bacitracin have been reported.[13]

Common and mild adverse effects of bacitracin include:

  • Fever
  • Hives
  • Itching
  • Swelling of lips and face [2]
  • Difficulty breathing
  • Nausea
  • Vomiting [14]
  • Allergic contact dermatitis [15]

Contraindications

Topical bacitracin is contraindicated in anyone with hypersensitivity to bacitracin or its formulation components. Patients with known hypersensitivity to neomycin may also be sensitive to bacitracin. Anaphylactoid reactions have been reported.[13]

Warnings and Precautions

  • Bacitracin application to an infection or wound caused by a viral or fungal infection may increase the risk of developing drug-resistant bacteria.
  • Topical bacitracin use is recommended only for minor skin injuries and should not be used over larger areas of the body.
  • Before using topical bacitracin, physician consultation is recommended for serious injuries such as burns, deep wounds, puncture wounds, or animal bites.[16][17]
  • In 2020, the FDA prohibited the use of bacitracin-containing injections because of the potential for nephrotoxicity.[18][19][20]

Monitoring

Secondary infections may develop; topical bacitracin should not be used for more than 7 days unless directed by a physician. The area of application should be monitored. If symptoms worsen, bacitracin use should be stopped immediately, and a clinician should be contacted regarding further management.[13]

Allergy patch testing may be necessary if an adverse reaction occurs after using bacitracin, either as a single-agent ointment or as part of a triple-therapy ointment. There have been multiple reports of anaphylactoid reactions and anaphylaxis associated with its use.[21][22][21] Furthermore, MRGPRX2, which belongs to a novel subfamily of G protein-coupled receptors (GPCRs) known as MAS-related GPCRs (MRGPRs), has been identified as a potential mediator in non-immunoglobulin E (IgE)-mediated responses. A study has shown that bacitracin can trigger MRGPRX2-dependent activation of mast cells, suggesting that non-IgE-mediated mechanisms may contribute to pseudo-allergic drug hypersensitivity reactions. This finding offers insights into the mechanism behind bacitracin-induced allergic contact dermatitis, underscoring the need for more research to thoroughly investigate and establish effective treatment options.[23]

Toxicity

Signs and Symptoms of Overdose

No toxicity is reported with the topical use of bacitracin, either as a single agent or in a triple therapy ointment. However, the intramuscular route has been associated with nephrotoxicity and renal failure due to tubular and glomerular necrosis. Consequently, careful monitoring is essential for intramuscular administration of bacitracin. Renal function should be assessed before, during, and after intramuscular administration to ensure safety.

Management of Overdose

Patients' daily optimal fluid intake and urinary output should be closely monitored to prevent kidney injury. Concurrent use of nephrotoxic drugs such as streptomycin, kanamycin, polymyxin E, and neomycin should be avoided.[24][25]

Enhancing Healthcare Team Outcomes

Topical bacitracin has been widely available and recognized as a safe over-the-counter topical antibiotic for the past 7 decades.[2] However, its increased use and adverse effects led to its designation as the "contact allergen of the year" in 2003 by the American Contact Dermatitis Society.[26] Between 2005 and 2006, it was identified as the sixth most common allergen in patch tests.[27][28] All healthcare professionals should be vigilant about the potential risks of anaphylactoid reactions or anaphylaxis associated with bacitracin use. Individuals with confirmed contact dermatitis should avoid products containing bacitracin. Healthcare providers should advise patients to carefully read labels for bacitracin in ointments, creams, and other wound care products.

Healthcare providers should consider bacitracin as a potential cause when encountering a patient with a possible contact allergy, persistent dermatitis, or a non-healing wound, as bacitracin allergy may mimic cellulitis or superficial wound infection. A clinical indicator distinguishing an allergic reaction from an infectious process is the presence of itching in allergic responses, as opposed to worsening pain in infections. Collaboration between dermatologists and immunologists can provide insights into distinguishing allergic dermatitis from infection. In cases of anaphylaxis caused by bacitracin, emergency medicine physicians should promptly stabilize the patient. Bacitracin should be used with caution in patients with pre-existing renal impairment or renal failure. To ensure patient safety, an interprofessional team approach involving physicians, nurses, and pharmacists is essential to monitor patients' fluid intake, urinary output, and renal function. Due to the significant risk of nephrotoxicity, pharmacists should suggest alternative medication options when available. Effective communication among clinicians (MDs, DOs, NPs, PAs), pharmacists, nurses, and specialists is crucial to optimizing patient outcomes with topical bacitracin treatment.

Review Questions

References

1.
WRONG NM, SMITH RC, HUDSON AL, HAIR HC. The treatment of pyogenic skin infections with bacitracin ointment. Treat Serv Bull. 1951 Jun;6(6):257-61. [PubMed: 14835814]
2.
Schalock PC, Zug KA. Bacitracin. Cutis. 2005 Aug;76(2):105-7. [PubMed: 16209155]
3.
Varu DM, Rhee MK, Akpek EK, Amescua G, Farid M, Garcia-Ferrer FJ, Lin A, Musch DC, Mah FS, Dunn SP., American Academy of Ophthalmology Preferred Practice Pattern Cornea and External Disease Panel. Conjunctivitis Preferred Practice Pattern®. Ophthalmology. 2019 Jan;126(1):P94-P169. [PubMed: 30366797]
4.
Ma Y, Zhang N, Wu S, Huang H, Cao Y. Antimicrobial activity of topical agents against Propionibacterium acnes: an in vitro study of clinical isolates from a hospital in Shanghai, China. Front Med. 2016 Dec;10(4):517-521. [PubMed: 27896620]
5.
McDonald LC, Gerding DN, Johnson S, Bakken JS, Carroll KC, Coffin SE, Dubberke ER, Garey KW, Gould CV, Kelly C, Loo V, Shaklee Sammons J, Sandora TJ, Wilcox MH. Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA). Clin Infect Dis. 2018 Mar 19;66(7):e1-e48. [PMC free article: PMC6018983] [PubMed: 29462280]
6.
Johnson BA, Anker H, Meleney FL. BACITRACIN: A NEW ANTIBIOTIC PRODUCED BY A MEMBER OF THE B. SUBTILIS GROUP. Science. 1945 Oct 12;102(2650):376-7. [PubMed: 17770204]
7.
Heal CF, Banks JL, Lepper PD, Kontopantelis E, van Driel ML. Topical antibiotics for preventing surgical site infection in wounds healing by primary intention. Cochrane Database Syst Rev. 2016 Nov 07;11(11):CD011426. [PMC free article: PMC6465080] [PubMed: 27819748]
8.
Stone KJ, Strominger JL. Mechanism of action of bacitracin: complexation with metal ion and C 55 -isoprenyl pyrophosphate. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3223-7. [PMC free article: PMC389626] [PubMed: 4332017]
9.
Ray P, Singh S, Gupta S. Topical antimicrobial therapy: Current status and challenges. Indian J Med Microbiol. 2019 Jul-Sep;37(3):299-308. [PubMed: 32003326]
10.
Gigliotti F, Hendley JO, Morgan J, Michaels R, Dickens M, Lohr J. Efficacy of topical antibiotic therapy in acute conjunctivitis in children. J Pediatr. 1984 Apr;104(4):623-6. [PubMed: 6323667]
11.
Leachman SA, Reed BR. The use of dermatologic drugs in pregnancy and lactation. Dermatol Clin. 2006 Apr;24(2):167-97, vi. [PubMed: 16677965]
12.
Murase JE, Heller MM, Butler DC. Safety of dermatologic medications in pregnancy and lactation: Part I. Pregnancy. J Am Acad Dermatol. 2014 Mar;70(3):401.e1-14; quiz 415. [PubMed: 24528911]
13.
Cronin H, Mowad C. Anaphylactic reaction to bacitracin ointment. Cutis. 2009 Mar;83(3):127-9. [PubMed: 19363904]
14.
Sheth VM, Weitzul S. Postoperative topical antimicrobial use. Dermatitis. 2008 Jul-Aug;19(4):181-9. [PubMed: 18674453]
15.
Maury CA, Gruson KI, Tabeayo E, Gruson LM, Merchan ECR. Allergic Contact Dermatitis (ACD) to Topical Products in Orthopedic Surgery: Clinical Characteristics and Treatment Strategies. Arch Bone Jt Surg. 2023;11(10):604-616. [PMC free article: PMC10590484] [PubMed: 37873527]
16.
Jones RN, Li Q, Kohut B, Biedenbach DJ, Bell J, Turnidge JD. Contemporary antimicrobial activity of triple antibiotic ointment: a multiphased study of recent clinical isolates in the United States and Australia. Diagn Microbiol Infect Dis. 2006 Jan;54(1):63-71. [PubMed: 16368476]
17.
Bonomo RA, Van Zile PS, Li Q, Shermock KM, McCormick WG, Kohut B. Topical triple-antibiotic ointment as a novel therapeutic choice in wound management and infection prevention: a practical perspective. Expert Rev Anti Infect Ther. 2007 Oct;5(5):773-82. [PubMed: 17914912]
18.
Roy N, Oleru O, Amakiri U, Stratis C, Kwon D, Wang A, Akhavan A, Henderson PW. Outcomes After Implant-Based Breast Reconstruction Following the National Institution of a Ban on Bacitracin Irrigation. Ann Plast Surg. 2024 Apr 01;92(4S Suppl 2):S191-S195. [PMC free article: PMC10984754] [PubMed: 38319958]
19.
Oleru OO, Akhavan AA, Seyidova N, Ibelli T, Taub PJ, Henderson P. Did the National Ban on Bacitracin Irrigation Affect Infection Rates in Implant-Based Breast Reconstruction? An Analysis of a National Database. Clin Breast Cancer. 2023 Apr;23(3):e103-e108. [PMC free article: PMC11000432] [PubMed: 36658063]
20.
Gu Y, Song S, Zhu Q, Jiao R, Lin X, Yang F, van der Veen S. Bacitracin enhances ceftriaxone susceptibility of the high-level ceftriaxone-resistant gonococcal FC428 clone. Microbiol Spectr. 2023 Dec 12;11(6):e0244923. [PMC free article: PMC10715023] [PubMed: 37982635]
21.
Katz BE, Fisher AA. Bacitracin: a unique topical antibiotic sensitizer. J Am Acad Dermatol. 1987 Dec;17(6):1016-24. [PubMed: 2963037]
22.
Saryan JA, Dammin TC, Bouras AE. Anaphylaxis to topical bacitracin zinc ointment. Am J Emerg Med. 1998 Sep;16(5):512-3. [PubMed: 9725969]
23.
Yang F, Limjunyawong N, Peng Q, Schroeder JT, Saini S, MacGlashan D, Dong X, Gao L. Biological screening of a unique drug library targeting MRGPRX2. Front Immunol. 2022;13:997389. [PMC free article: PMC9635925] [PubMed: 36341461]
24.
Levin HS, Kagan BM. Antimicrobial agents: pediatric dosage, routes of administration and preparation procedures for parenteral therapy. Pediatr Clin North Am. 1968 Feb;15(1):275-90. [PubMed: 4295551]
25.
KOCH R, DONNELL G. Staphylococcic infections in children. Calif Med. 1957 Nov;87(5):313-6. [PMC free article: PMC1512125] [PubMed: 13472470]
26.
Sood A, Taylor JS. Bacitracin: allergen of the year. Am J Contact Dermat. 2003 Mar;14(1):3-4. [PubMed: 14744414]
27.
Spring S, Pratt M, Chaplin A. Contact dermatitis to topical medicaments: a retrospective chart review from the Ottawa Hospital Patch Test Clinic. Dermatitis. 2012 Sep-Oct;23(5):210-3. [PubMed: 23010827]
28.
Zug KA, Warshaw EM, Fowler JF, Maibach HI, Belsito DL, Pratt MD, Sasseville D, Storrs FJ, Taylor JS, Mathias CG, Deleo VA, Rietschel RL, Marks J. Patch-test results of the North American Contact Dermatitis Group 2005-2006. Dermatitis. 2009 May-Jun;20(3):149-60. [PubMed: 19470301]

Disclosure: Rosalee Nguyen declares no relevant financial relationships with ineligible companies.

Disclosure: Niloufar Khanna declares no relevant financial relationships with ineligible companies.

Disclosure: Anthony Safadi declares no relevant financial relationships with ineligible companies.

Disclosure: Preeti Patel declares no relevant financial relationships with ineligible companies.

Disclosure: Yan Sun declares no relevant financial relationships with ineligible companies.

Copyright © 2024, StatPearls Publishing LLC.

This book is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits others to distribute the work, provided that the article is not altered or used commercially. You are not required to obtain permission to distribute this article, provided that you credit the author and journal.

Bookshelf ID: NBK536993PMID: 30725678

Views

  • PubReader
  • Print View
  • Cite this Page

Related information

  • PMC
    PubMed Central citations
  • PubMed
    Links to PubMed

Similar articles in PubMed

See reviews...See all...

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...