PROLAYED LIDOCAINE MALE GENITAL DESENSITIZER- lidocaine ointment 
ViaDerma Distribution, Inc.

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Prolayed Lidocaine Ointment-Male Genital Desensitizer

Drug Facts

Active Ingredient

Lidocaine 10 mg

Purpose

Male genital desenitizer

Use

Helps in temporarily slowing the onset of 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 medical supervision
  • you or your partner develop a rash or irritation, such as burning or itching.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive Ingredients

acetic acid, ascorbic acid, chlorhexidine gluconate, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl-cellulose, magnesium stearate, methylparaben, sodium hydroxide, sorbic acid, stearic acid, water

Package Labeling:

Outer Package2Inner Package2

PROLAYED LIDOCAINE MALE GENITAL DESENSITIZER 
lidocaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71262-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SORBIC ACID (UNII: X045WJ989B)  
ACETIC ACID (UNII: Q40Q9N063P)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCERIN (UNII: PDC6A3C0OX)  
HISTIDINE (UNII: 4QD397987E)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71262-006-151 in 1 BOX06/23/2017
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/23/2017
Labeler - ViaDerma Distribution, Inc. (081113521)

Revised: 12/2023
Document Id: 0b81a020-0873-e454-e063-6294a90a2e03
Set id: 9c5ad0d0-ca7a-4321-9334-f06f3f6be18f
Version: 3
Effective Time: 20231202
 
ViaDerma Distribution, Inc.