POWERECT BENZOCAINE MALE DELAY GEL- benzocaine gel 
SKINS SEXUAL HEALTH LIMITED

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POWERECT Benzocaine Male Delay Gel

DRUG FACTS

ACTIVE INGREDIENT:

Benzocaine 5.00%

Purpose:

Male genital desensitizer

USES:

Helps to temporarily prevent premature ejaculation.

WARNINGS:

Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician.

FOR EXTERNAL USE ONLY.Avoid contact with eyes.

Keep out of reach of children.

If product is swallowed, get medical attention or contact poison control center immediately.

DIRECTIONS:

Apply product to the head and shaft of the penis prior to intercourse, or as directed by your physician. Wipe away excess product.

INACTIVE INGREDIENTS:

Aqua (deionized Water), Ethylhexylglycerin, Hydroxyethylcellulose, l-Arginine, Lepidium Meyenii (Maca) Extract, Panax Ginseng Root Extract, PEG-8, Phenoxyethanol, Propylene Glycol.

OTHER INFORMATION:

Store in a cool dry place below 30°C (86°F) out of direct sunlight.

QUESTIONS?

Contact us on +44 1636 593943

Package Labeling:3ml

Bottle5

Package Labeling:15ml

Bottle6

POWERECT BENZOCAINE MALE DELAY GEL 
benzocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81923-367
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
ARGININE (UNII: 94ZLA3W45F)  
ASIAN GINSENG (UNII: CUQ3A77YXI)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81923-367-003 mL in 1 PACKET; Type 0: Not a Combination Product10/03/2022
2NDC:81923-367-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product10/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/03/2022
Labeler - SKINS SEXUAL HEALTH LIMITED (221947744)

Revised: 11/2023
Document Id: 0976edf3-b970-fff9-e063-6294a90a2c4e
Set id: 2fafe1f2-a31e-4b2a-bc51-81e16b319c3a
Version: 2
Effective Time: 20231106
 
SKINS SEXUAL HEALTH LIMITED