What is the recommended dose of Kenalog (triamcinolone) injection for treating dermatitis skin lesions?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 5, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Kenalog Injection Dose for Dermatitis Skin Lesions

For dermatitis skin lesions, use intralesional triamcinolone acetonide at a concentration of 2.5 mg/mL, injecting 0.05 mL per lesion into the center of the inflammatory lesion. 1, 2

Concentration and Volume

  • The standard concentration is 2.5 mg/mL, which represents the most commonly used dilution among dermatologists (52.5% of practitioners) and has demonstrated virtually 100% effectiveness in localized inflammatory dermatoses 2, 3

  • Inject 0.05 mL per lesion, which is the most frequently used volume (42.3% of practitioners) and provides adequate therapeutic effect while minimizing adverse events 2

  • The original formulation comes at 10 mg/mL and should be diluted with sterile normal saline to achieve the 2.5 mg/mL concentration 1

Injection Technique

  • Inject into the center of the lesion at the dermal level, as practiced by 61.6% of dermatologists surveyed 2

  • Use low-pressure injection technique to minimize risk of complications 3

  • Avoid injecting at sites of active infection such as impetigo or herpes 1

Total Dosing Limits

  • Maximum safe dose is 15-20 mg (6-8 cc at 2.5 mg/mL concentration) every 3-4 weeks for patients over 50 kg 3

  • The usual maximum per session is 7.5 mg (3 cc at 2.5 mg/mL) for most patients 3

  • Multiple lesions can be treated in one session as long as total dose remains within these limits 3

Expected Response and Follow-up

  • Reassess after 2 weeks to evaluate treatment response 1

  • Most inflammatory dermatitis lesions respond within this timeframe with significant improvement in erythema, induration, and pruritus 4

  • If no improvement occurs after 2 weeks, consider alternative diagnoses or treatment modalities 1

Critical Safety Considerations

  • Counsel patients about hypopigmentation and atrophy risk before every injection, as recommended by 50.5% of practitioners 2

  • Atrophy, when it occurs, typically lasts over 6 months (48.4% of cases), though the overall incidence is extremely low (<1% of patients) 2

  • Contraindications include hypersensitivity to triamcinolone, active tuberculosis, uncontrolled diabetes, severe hypertension, and active peptic ulcer disease 1

  • Monitor for signs of hypothalamic-pituitary-adrenal axis suppression with repeated injections, particularly when approaching maximum dosing limits 1, 3

Common Pitfalls to Avoid

  • Do not use concentrations higher than 2.5 mg/mL for dermatitis lesions, as higher concentrations (such as the 10-40 mg/mL used for keloids and hypertrophic scars) significantly increase atrophy risk 1

  • Avoid superficial injection, which increases risk of visible atrophy and hypopigmentation 2

  • Do not inject into areas with impaired wound healing or recent facial surgery with extensive undermining 1

  • Ensure proper dilution technique, as using the wrong concentration is a frequent source of adverse events 1, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Dermatologist Use of Intralesional Triamcinolone in the Treatment of Acne.

The Journal of clinical and aesthetic dermatology, 2020

Research

Update on intralesional steroid: focus on dermatoses.

Journal of cutaneous medicine and surgery, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.