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EJECTDELAY by Innovus Pharmaceuticals, Inc.

Medically reviewed on November 13, 2017

Dosage form: gel
Ingredients: Benzocaine 7.5g in 100g
Labeler: Innovus Pharmaceuticals, Inc.
NDC Code: 57483-003

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.

Drug Facts

Active Ingredients

Benzocaine 7.5%

Purpose

Male genital desensitizer

Indications

Helps in the prevention of premature ejaculation

Warnings

For external use only

When using this product

Avoid contact with eyes

Stop use and ask a doctor if
  • Premature ejaculation may be due to a condition requiring medical supervision
  • This product, used as directed, does not provide relief, discontinue use and consult a physician
  • You or your partner develop a rash or irritation, such as burning or itching, discontinue use
  • If symptoms persist, consult a doctor

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 physician.

Wash product off after intercourse

Inactive Ingredients

Glycerin Natural USP Kosher, PEG 8 Pluracol E 400 NF, PEG 3350, PEG 540 Blend USP, Carbowax 4000, Sodium Saccharin Powder USP, Sorbic Acid, Water

Questions or Comments

For questions or comments please call 1-858-964-5123

EJECTDELAY  GEL
benzocaine 7.5% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57483-003
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (Benzocaine) Benzocaine7.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Glycerin 
POLYETHYLENE GLYCOL 400 
POLYETHYLENE GLYCOL 3350  
POLYETHYLENE GLYCOL 4000  
SACCHARIN SODIUM  
SORBIC ACID  
Water 
Packaging
#Item CodePackage Description
1NDC:57483-003-021 TUBE (TUBE) in 1 BOX
1NDC:57483-003-0356.8 g in 1 TUBE
2NDC:57483-003-065 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B07/15/2013
Labeler - Innovus Pharmaceuticals, Inc. (962507187)
Registrant - Innovus Pharmaceuticals, Inc. (962507187)
Establishment
NameAddressID/FEIOperations
U.S. Pharmaceuticals, Inc.009248480manufacture(57483-003)

 
Innovus Pharmaceuticals, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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