Label: INSTANT ERECTION- ultimate erection enhancer cream

  • NDC Code(s): 83608-104-02, 83608-104-05
  • Packager: Novelties by Nasswalk, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 Label Information

Updated August 24, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient:

    Benzocaine 5%

  • Purpose:

    Desensitizer

  • Uses:

    Desentisizes the Penis, and allows an erection to be maintained.

  • Warnings:

    For External use only. Do not use near eyes. Not for prolonged use. If condition for which preparation is used causes discomfort, or if a rash or irritation should develop, discontinue use and consult a physician. For prevention of premature ejaculation.

  • Keep out of reach of children.

  • Directions:

    Apply a small amount of cream to head and shaft of penis 2-3 minutes before intercourse. Wash product off after intercourse.

  • Inactive Ingredients:

    Water, Stearic Acid, Propylene Glycol, Glycerin, Mineral Oil, Stearyl Alcohol, Glyceryl Stearate SE, Petrolatum, Sodium Lauryl Sulfate, Aminomethyl Propanediol, Phenoxyethanol, Ethylhexylglycerin.

  • INSTANT ERECTION CREAM

    INSTANT ERECTION CREAM

    ULTIMATE ERECTION ENHANCER

    Net Wt. 0.5 oz.

    Made in USA

    Distributed By: Novelties by Nasswalk Inc, North Bergeb, NJ 07047. WWW.NASSTOYS.COM

    Tube:

    Tube

    Carton:

    Unit Carton-1

    INSTANT ERECTION CREAM

    Net Wt. 0.5 oz.

    Made in USA

    Distributed By: Novelties by Nasswalk Inc, North Bergeb, NJ 07047. WWW.NASSTOYS.COM

    Carton:

    Unit Carton-2

  • INGREDIENTS AND APPEARANCE
    INSTANT ERECTION 
    ultimate erection enhancer cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83608-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83608-104-051 in 1 CARTON08/07/2023
    10.5 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:83608-104-021 in 1 CARTON08/07/2023
    20.5 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/07/2023
    Labeler - Novelties by Nasswalk, Inc. (049455157)
    Registrant - Novelties by Nasswalk, Inc. (049455157)
    Establishment
    NameAddressID/FEIBusiness Operations
    Advance Cosmetics Research Laboratories Inc,874810872manufacture(83608-104)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!