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 944 Corp. 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 Ingredients
Benzocaine USP 4.0%
Purpose
Male Genital Desensitizer
Use
Helps in temporarily prolonging time until ejaculation.
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 develop 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 – Pouch Label
PREBOOST™
MALE DESENSITIZING WIPES
Helps in temporarily
prolonging time until ejaculation
Developed by Dr. Harry Fisch
www.preboost.com
1 single-use premoistened towelette
Manufactured for 944 Corp
944 Park Ave, New York, NY 10028 www.preboost.com
Principal Display Panel – Box Label
PREBOOST™
MALE DESENSITIZING WIPES
Helps in temporarily prolonging time until ejaculation
10 single-use
premoistened towelette
Developed by Dr. Harry Fisch
|www.preboost.com
* Please review the disclaimer below.