Active Ingredient
Bezocaine 5%
The following Structured Product Label (SPL) was submitted to the FDA by Guoyu Trading Co., Ltd. for the product Nekvnro Anti-itch Creme (NDC 84844-007). 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 ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Bezocaine 5%
External analgesic
temporarily relieves itching
For external use only
Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.
THIS PRODUCT Avoid contact with eyes
Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.
Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.
lf swallowed, get medical help or contact a Poison Control Center right away.
adults and children 12 years and older apply a fingertipamount (approximately 1-inch strip) to affected area not more than 3 to 4times daily.Clean nozzle of tube by wiping thoroughly before replacing cap.Keep cap tightly closed between uses.
children under 12 years consult a doctor
Glycerol 、Propylene Glycol 、Polydimethylsiloxane 、Trolaminewater、Boreol 、MENTHA PIPERITA、Methylparaben 、Chlorhexidine
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