Dzeus Climax Control Wipes
FDA Label NDC 54723-006
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sambria Pharmaceuticals, Llc for the product Dzeus Climax Control Wipes (NDC 54723-006). 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 facts, active ingredient, purpose, uses, warnings, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzocaine USP 7%
Purpose
Male genital Sensitizer
Uses
- Aids in the prevention of premature Ejaculation
- Aids in temporarily prolonging the time until ejaculation
Warnings
For External Use only
Do not use on broken or inflamed skin
If pregnant or breastfeeding, ask a health professional before use
When using this product, avoid contact with eyes
Stop and ask doctor if:
This product, when used as directed, does not provide relief; premature ejaculation may be due to a condition requiring medical supervision
you or your partner develop rash or irritation, such as burning or itching symptoms persist
Keep Out Of Reach Of Children
In case of ingestion, seek professional assistance and contact poison control immediately
Directions
Use wipe to apply a small amount of product to the head and shape of the penis before intercourse, or as directed by a doctor. Was off after intercourse
Allow product to dry prior to intercourse
Not suitable for oral use
Use as directed
Other Information
Store between 20°-25 °C (68°-77 °F)
Inactive Ingredients
Lactic Acid, Phenol, Phenoxyethanol, ethylhexylglycerin, Polyethylene Glycol, purified water
Product Label
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