Active Ingredient
Benzocaine USP 4%
Intimate Wipe
FDA Label NDC 69681-434
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Veru Inc. for the product Intimate Wipe (NDC 69681-434). 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 active ingredient, purpose, use, warnings, otc - when using, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Male Genital Desensitizer
Use
Helps in temporarily prolonging time until ejaculation
Warnings
For external use only
Otc - When Using
When using this product avoid contact with the eyes.
Stop Use And Ask A Doctor If
- this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring supervision.
- You or your partner develop a rash or irritation, such as burning or itching
- Symptoms persist.
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.
Inactive Ingredients
ethyl alcohol (SDA 40B), propylene glycol, purified water
Principal Display Panel – Box Label
PLAYBOY
INTIMATE WIPES
MALE GENITAL DESENSITIZER
Alright, Alright, All Night
Climax Delaying
Benzocaine Formulation
Fragrance & Paraben-Free
4 INDIVIDUALLY WRAPPED
CLIMAX DELAYING WIPES
Figure (Pla02 0000 01)
Principal Display Panel – Packet Label
PLAYBOY
INTIMATE WIPES
MALE GENITAL DESENSITIZER
1 INDIVIDUALLY WRAPPED
CLIMAX DELAYING WIPE
Figure (Pla02 0000 02)
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