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Triethanolamine Salicylate

Prescription

品牌名称: Salicor

剂型
Patch
给药途径
TRANSDERMAL
生产厂商
Clinic Pharma

About This Medication

DESCRIPTION Salicor™ is an external analgesic product containing 10% triethanolamine salicylate as the active ingredient. Triethanolamine salicylate is an organic compound formed between triethanolamine and salicylic acid, where triethanolamine neutralizes the acidity of salicylic acid. This external analgesic is designed for temporary relief of minor pain associated with arthritis, simple backache, muscle strains, sprains, and bruises. Unlike other external analgesics, triethanolamine salicylate has no distinct odor, which improves patient acceptability.

活性成分

成分 规格
Tea-Salicylate -

适应证与用法

INDICATION AND USAGE Salicor™ is indicated for the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, muscle strains and sprains, bruises, bursitis, and dysmenorrhea. Salicor™ provides a localized analgesic effect directly at the site of pain, offering convenience and sustained relief compared to cream formulations.

用法用量

DOSAGE AND ADMINISTRATION For adults 18 years and older: • Clean and dry the affected area • Locate the tear notch on the edge of the pouch. Tear open at the notch or carefully cut open the pouch with scissors, taking care not to cut the system inside • Remove the transparent release liner before applying Salicor™ to the skin • Apply one Salicor™ to the affected area of pain and leave it in place for 8 to 12 hours • Apply only one Salicor™ at a time • If pain persists, the used Salicor™ may be replaced with a new one for up to 8 to 12 more hours • Always remove and properly dispose of the used Salicor™ before applying a new one • Salicor™ may be cut into smaller sizes with scissors prior to removing the release liner • Safely discard the used Salicor™ (whole or cut pieces) where children and pets cannot access it • Wash hands with soap and water after applying or removing Salicor™ Visual Guide provided below: These highlights do not include all the information needed to use Salicor™ safely and effectively. See full prescribing information for Salicor™ dosing

警告与注意事项

药代动力学

Pharmacokinetics Absorption Following external administration of Salicor™ to healthy volunteers, no detectable levels of salicylic acid were found in the serum, indicating low systemic absorption. This minimal absorption is advantageous as it reduces the risk of systemic side effects commonly associated with oral salicylates. Studies have shown that urinary recovery of total salicylate during the first 24 hours after external application was only 6.9 mg, which represents approximately 1.4% of the total dose applied. Distribution Triethanolamine salicylate is transported and distributed within cells and tissues through various mechanisms. Studies in canines and humans have shown that transdermal absorption of salicylate from triethanolamine salicylate preparations applied to skin is consistent and reproducible, with measurable tissue salicylate levels at the application site. The distribution appears to be concentration-dependent, with tissue salicylate levels directly proportional to the concentrations of the active ingredient in the formulation up to the 10% preparation. Metabolism While specific metabolism data for externally applied Salicor™ is limited due to its low systemic absorption, the small amount that does enter the systemic circulation is likely metabolized similarly to other salicylates. The primary metabolic pathways include: 1. Conjugation with glycine to form salicyluric acid (approximately 75%). 2. Conjugation with glucuronic acid to produce salicyl acyl and phenolic glucuronides (about 15%). 3. Oxidation to gentisic acid and other hydroxylated derivatives (minor pathway). Free, unmodified salicylate accounts for 10–30% of excreted metabolites, depending on dosage and individual factors like urinary pH. Metabolism primarily occurs in the liver, with some possible local metabolism in skin tissues. Excretion Triethanolamine salicylate is primarily excreted through the urine after metabolism. Following external application of a 10% formulation, approximately 1.4% of the total dose is recovered in the urine as salicylate within the first 24 hours, indicating low systemic absorption.

Frequently Asked Questions

INDICATION AND USAGE Salicor™ is indicated for the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, muscle strains and sprains, bruises, bursitis, and dysmenorrhea. Salicor™ provides a localized analgesic effect directly at the site of pain, offering convenience and sustained relief compared to cream formulations.

DOSAGE AND ADMINISTRATION For adults 18 years and older: • Clean and dry the affected area • Locate the tear notch on the edge of the pouch. Tear open at the notch or carefully cut open the pouch with scissors, taking care not to cut the system inside • Remove the transparent release liner before applying Salicor™ to the skin • Apply one Salicor™ to the affected area of pain and leave it in place for 8 to 12 hours …

PRECAUTIONS General If irritation or a burning sensation occurs during application, wash the product off your skin and do not reapply until the irritation subsides. When Salicor™ is used concomitantly with other products containing local anesthetic agents, the amount absorbed from all formulations must be considered. Stop use and ask a doctor if • Condition worsens • Symptoms persist for more than 7 days, or symptoms return within a few days after discontinuing use • Redness is present • Irritation …

Triethanolamine Salicylate is a prescription medication. You will need a valid prescription from a licensed healthcare provider.

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References & Data Sources

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本页面信息仅供教育参考之用,不得用于替代专业医疗建议、诊断或治疗。

如有任何关于病症或药物的疑问,请务必咨询您的医生或其他具有资质的医疗保健提供者。

数据来源: DailyMed (NLM), openFDA, MFDS

Medical Disclaimer

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.