Boy Butter
FDA Label NDC 24488-043

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Boy Butter Lubes for the product Boy Butter (NDC 24488-043). 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, indications:, keep out of reach of children, warnings:, directions:, inactive ingredients:, questions or comments:, 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

Indications:

Helps in the prevention of premature ejaculation.

  • For temporary male genital desensitization, helping to slow the onset of ejaculation
  • Helps in temporarily slowing the onset of ejaculation
  • For reducing oversensitivity in the male in advancer of intercourse.

Keep Out Of Reach Of Children

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

Warnings:

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 physician
  • Avoid contact with the eye. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use
  • If symptoms persist, consult a physician.

Directions:

Apply a small amount to head and shaft of penis before intercourse, or use as directed by a physician

  • Wash product off after intercourse

Inactive Ingredients:

Water, Petrolatum, Propylene Glycol, Cyclopentasiloxane, Mineral Oil, Glyceryl Stearate Se, Polysorbate 60, Glycol Distearate, Coconut Oil, Germall 11, Methyparaben, Propylparaben, Yellow 5

Questions Or Comments:

For questions or comments, please call 1-818-888-6825

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