INTIMATE WIPE- benzocaine liquid

Intimate Wipe by

Drug Labeling and Warnings

Intimate Wipe by is a Otc medication manufactured, distributed, or labeled by Veru Inc., Safetec of America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Principal Display Panel – Packet Label

PLAYBOY

INTIMATE WIPES

MALE GENITAL DESENSITIZER

1 INDIVIDUALLY WRAPPED

CLIMAX DELAYING WIPE

INGREDIENTS AND APPEARANCE

INTIMATE WIPE 
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69681-434
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5)	benzocaine	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
alcohol (UNII: 3K9958V90M)
water (UNII: 059QF0KO0R)
propylene glycol (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69681-434-04	4 in 1 BOX	06/08/2020
1		1.2 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	06/08/2020

Labeler - Veru Inc. (055300578)

Registrant - Safetec of America, Inc. (874965262)