Otc - Active Ingredient
Benzocaine 7.5%
The following Structured Product Label (SPL) was submitted to the FDA by Cc Wellness Llc for the product Lubelife Climax Control Delay (NDC 71683-005). 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 otc - active ingredient, otc - purpose, uses:, ask a doctor before use:, when using this product, directions:, other information:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzocaine 7.5%
Male Genital Desensitizer
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.
Can be used for sexual intercourse and sex play when applied in accordance with usage instructions. Only use in accordance with the instructions, seek medical attention immediately in case of overdose.
PEG-8, Propylene Glycol, Water (Aqua)
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