Thunder Fck Male Genital Desensitizer Liquid
FDA Label NDC 70742-587

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Product Max Group Inc for the product Thunder Fck Male Genital Desensitizer (NDC 70742-587). 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, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzocaine 7.5%

Purpose

Male Genital Desensitizer

Uses

  • Helps in the prevention of premature ejaculation.

Warnings

For external use only.

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.

Avoid contact with the eyes.

If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poision Control Center right away.

Directions

  • Apply a small amount to the head and shaft of the penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

Other Information

  • Store between 20-30°C (68-86°F)

Inactive Ingredients

Alcohol, Propylene Glycol, PEG-8, Polysorbate 20, Phenoxyethanol, Ethylhexylglycerin, Cannabis Sativa Seed Oil

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