Magic Stamina
FDA Label NDC 70742-088

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 Magic Stamina (NDC 70742-088). 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 drug factsactive 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

Drug Factsactive Ingredient

Benzocaine 5%

Purpose

Male Genital Desensitizer

Uses

Helps in the prevention of premature ejaculation.

Warnings

For external use only.

  • Avoid contact with eyes
  • 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.

Keep Out Of Reach Of Children

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

Directions

  • Apply a small amount to head and shaft of penis before intercourse.
  • Wash product off after intercourse.

Other Information

Do not use if safety tab is broken or missing.

Inactive Ingredients

Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water

Magic Stamina Product Label

Benzocaine Male genital Desensitizer

Magic STAMINA®

Climax contral spray

1.0 FL. OZ. (30 mL)

Distributed By: Body Action Products, Lutz FL 33559

www.bodyactionproducts.com

* Please review the disclaimer below.