FDA Label for Preboost

View Indications, Usage & Precautions

Preboost Product Label

The following document was submitted to the FDA by the labeler of this product The Female Health Company D/b/a Veru Healthcare. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Other



Drug Facts


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"


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