HIGHER CONTROL MALE CLIMAX CONTROL LUBRICATING- benzocaine gel 
Product Max Group Inc

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HIGHER CONTROL Male Climax Control Lubricating

Drug Facts

Active Ingredient

Benzocaine 5%

Purpose

Male Genital Desensitizer

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.

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.
  • Wash product off after intercourse.

Other Information

Do not use if safety seal is broken or missing.

Inactive Ingredients

Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Methylparaben, PEG-8, Polysorbate 20, Propylene Glycol, Propylparaben, Water.

Package Labeling:

Label2

HIGHER CONTROL MALE CLIMAX CONTROL LUBRICATING 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-181
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70742-181-022 mL in 1 PACKET; Type 0: Not a Combination Product03/01/201812/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/01/201812/31/2020
Labeler - Product Max Group Inc (134893911)

Revised: 10/2023
 
Product Max Group Inc