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Drug Facts
Preboost Liquid
FDA Label NDC 69681-432
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Female Health Company D/b/a Veru Healthcare for the product Preboost (NDC 69681-432). 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 other, active ingredient, purpose, use, otc - stop use, otc - keep out of reach of children, directions, inactives, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzocaine USP 4%
Purpose
Male Genital Desensitizer
Use
Helps in temporarily prolonging time until ejaculation
Otc - Stop Use
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.
- Avoid contact with the eyes.
- If you or your partner develops a rash or irritation, such as burning or itching, discontinue use.
- If symptoms persist, consult a doctor.
Otc - 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.
Directions
Apply a small amount to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.
Inactives
Purified water, Ethyl Alcohol (SDA 40B), Propylene Glycol
Principal Display Panel - 10 Wipes Packet Box
Clinically Proven to Make Sex Last Longer
PREBOOST®
KEEP IT GOING
10 Single-Use Wipes
Male desensitizing wipes for
prolonging the time until ejaculation
H Fisch MD
Created by Dr. Harry Fisch, Named
"One of America's Best Doctors"
Principal Display Panel (10 Wipes Packet Box)
* Please review the disclaimer below.
