Active Ingredient:
Benzocaine 5.00%
Powerect Benzocaine Male Delay Gel
FDA Label NDC 81923-367
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Skins Sexual Health Limited for the product Powerect Benzocaine Male Delay Gel (NDC 81923-367). 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:, uses:, warnings:, keep out of reach of children., directions:, inactive ingredients:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
Male genital desensitizer
Uses:
Helps to temporarily prevent premature ejaculation.
Warnings:
Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician.
FOR EXTERNAL USE ONLY.
Avoid contact with eyes. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician.
Keep Out Of Reach Of Children.
If product is swallowed, get medical attention or contact poison control center immediately.
Directions:
Apply product to the head and shaft of the penis prior to intercourse, or as directed by your physician. Wipe away excess product.
Inactive Ingredients:
Aqua (deionized Water), Ethylhexylglycerin, Hydroxyethylcellulose, l-Arginine, Lepidium Meyenii (Maca) Extract, Panax Ginseng Root Extract, PEG-8, Phenoxyethanol, Propylene Glycol.
Other Information:
Store in a cool dry place below 30°C (86°F) out of direct sunlight.
Questions?
Contact us on +44 1636 593943
Package Labeling:3Ml
Bottle5 (Bottle5)
Package Labeling:15Ml
Bottle6 (Bottle6)
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