Active Ingredients
- Ethyl Alcohol 2,5 %.........Topical Anesthetic
- Lidocaine HCl 5%............Topical Anesthetic
The following Structured Product Label (SPL) was submitted to the FDA by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As for the product Konicare 5% (NDC 73107-902). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, indications & usage, uses:, do not use, stop use and ask a doctor if,, if pregnant or breast feeding,, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
For temporary relief of pain
• On wounds or damaged skin
• In large quantities
• With a heating pad
• If you are allergic to any ingredients of this product
• Use only as directed
• Avoid contact with the eyes, mucous membranes or rashes
• Do not bandage tightly
• Skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
• Conditions worsen
• Symptoms persist for more than 7 days
• Symptoms clear up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away
If swallowed, get medical help or contact a Poison Control Center right away
Adults and children 12 years of age and older:
Children under 12 years of age:
Water, Citric Acid, Methy Hydroxy Benzoate, Benzalkonium Chloride.
* Please review the disclaimer below.