Body Action Products Prolong Lubricating Gel
FDA Label NDC 70742-288

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 Body Action Products Prolong Lubricating (NDC 70742-288). 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 otc - 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

Otc - Active Ingredient

Benzocaine 5%

Purpose

Male Genital Desensitizer

Uses

  • Helps in the prevention of premature ejaculation.

Warnings

For external use only.

  • Avoid contact with the 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 seal under cap is broken or missing.

Inactive Ingredients

Cellulose Thickener, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water.

Package Labeling:

Label3 (Label3)

Label3 (Label3)

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