Mint Rx Endurance Wipes
FDA Label NDC 77691-433

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pharmamedrx for the product Mint Rx Endurance Wipes (NDC 77691-433). 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, keep out of reach of children, use, warnings, stop use and ask a doctor if, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Benzocaine 5%

Purpose

Male genital desensitizer

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a poison control center right away

Use

Helps in temporarily prolonging time until ejaculation

Warnings

For external use ony

When using this product avoid contact with eyes

Stop Use And Ask A Doctor If

This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision

You or your partner develop a rash or irritation such as burning or itching

Symptoms persist

Directions

Wipe head and shaft of penis before intercourse or use as directed by a doctor.  Wash product off of penis after intercourse

Inactive Ingredients

Purified water, ethyl alcohol, glycerin, Vitamin E, phenoxyethanol

Mint Rx Endurance Wipesbenzocaine Usp 5%

8 Packet In 1 Box > 2 mL In 1 Packet (Mintrxendurancewipes)

8 Packet In 1 Box > 2 mL In 1 Packet (Mintrxendurancewipes)

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