Drug Factsactive Ingredient
Benzocaine 5%
Prolong
FDA Label NDC 70742-089
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 Prolong (NDC 70742-089). 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, keep out of reach of children, uses, warnings, 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
Purpose
Male Genital Desensitizer
Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed get medical help or contact a Poison Control Center right away.
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.
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
Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water
Prolong Product Label
www.bodyactionproducts.com
Distributed by:
Body Action Products
Lutz, FL 33559
ACTION BODY PRODUCTS
Benzocaine Male Genital Desensitizer
PROLONG
FOR MEN
Helps Prolong Sexual Pleasure
Lubricating Gel
2 FL OZ (60 ml)
* Please review the disclaimer below.
