INTIMATE WIPE- benzocaine liquid 
Veru Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Benzocaine USP 4%

Purpose

Male Genital Desensitizer

Use

Helps in temporarily prolonging time until ejaculation

Warnings

For external use only

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

Principal Display Panel – Packet Label

PLAYBOY

INTIMATE WIPES

MALE GENITAL DESENSITIZER

1 INDIVIDUALLY WRAPPED

CLIMAX DELAYING WIPE

Figure
INTIMATE WIPE 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69681-434
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
alcohol (UNII: 3K9958V90M)  
water (UNII: 059QF0KO0R)  
propylene glycol (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69681-434-044 in 1 BOX06/08/2020
11.2 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34806/08/2020
Labeler - Veru Inc. (055300578)
Registrant - Safetec of America, Inc. (874965262)

Revised: 6/2020
Document Id: 23cd886e-a975-42ec-baf5-6cbacf805d66
Set id: 48756768-4865-666e-6572-4c6976657321
Version: 1
Effective Time: 20200608
 
Veru Inc.