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STAY HARD

Medically reviewed by Drugs.com. Last updated on July 28, 2020.

Dosage form: gel
Ingredients: BENZOCAINE 2833mg in 60mL
Labeler: Product Max Group Inc
NDC Code: 70742-048

STAY HARD - 048

Drug Facts
Active Ingredient

Benzocaine 5%

Purpose

Male Genital Desensitizer

Keep out of reach of children

Keep out of reach of children.

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

Uses
  • Helps in the prevention of premature ejaculation.

Warnings

For external use only.

  • Avoid contact with the eyes.
  • Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor.
  • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor.

Directions
  • Apply a small amount to head and shaft of penis before intercourse.
  • Wash product off after intercourse.

Other Information

Do not use if safety seal under cap is broken or missing.

Inactive Ingredients

Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water

STAY HARD product Label

STAY HARD
LUBRICATING GEL

ACTION BODY PRODUCTS

Climax Control gel

Helps in Temporarily Prolonging the Time Until Ejaculation

Benzocaine Male Genital desensitizer

2 FL OZ (60 ml)

www.bodyaction products.com

Distributed by:

Body Action Products

Lutz, FL 33559

STAY HARD 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-048
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE2833 mg  in 60 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) 
METHYLPARABEN 
POLYETHYLENE GLYCOL 400 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Packaging
#Item CodePackage Description
1NDC:70742-048-0160 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34806/15/2016
Labeler - Product Max Group Inc (134893911)
Registrant - Product Max Group Inc (134893911)

Document Id: 99d902a0-4a3b-4391-9712-578c972b6d34
Set id: 448186dd-7f22-411d-8b98-f4575d93e606
Version: 1
Effective Time: 20160807
 
Product Max Group Inc

Further information

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

Medical Disclaimer