The following Structured Product Label (SPL) was submitted to the FDA by Absorption for the product Promescent Delay Wipes (NDC 55636-000). 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 warnings, directions, indications, active ingredients, inactive ingredient, questions?, keep out of reach of children, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Avoid contact with the eyes.
Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor.
If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.
Apply a small amount to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.
For reducing oversensitivity in the male in advance of intercourse.
For reducing oversensitivity in the male in advance of intercourse.
Benzocaine 7% Male Genital Desensitizer
Propylene glycol
Visit Promescent.com
Keep out of reach of children
Distributed by: Absorption Pharmaceuticals LLC, Las Vegas, NV 89118, USA. Phone 1-877-852-0106 for reporting serious adverse events associated with use of this product, or visit promescent.com
* Please review the disclaimer below.
