Preboost
Preboost is an FDA drug label for the active ingredient BENZOCAINE manufactured by The Female Health Company d/b/a Veru Healthcare administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20170407.
Generic: BENZOCAINE
Manufacturer: The Female Health Company d/b/a Veru Healthcare
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 69681-432
Application: part348
Effective: 20170407
Active Ingredients: Active Ingredient Benzocaine USP 4%
Indications & Usage
Use Helps in temporarily prolonging time until ejaculation
Dosage & Administration
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.
Contraindications
Not available.
Warnings
Warnings 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. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Adverse Reactions
Not available.