THUNDER FCK MALE GENITAL DESENSITIZER- benzocaine liquid

Thunder Fck Male Genital Desensitizer by

Drug Labeling and Warnings

Thunder Fck Male Genital Desensitizer by is a Otc medication manufactured, distributed, or labeled by PRODUCT MAX GROUP INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzocaine 7.5%

Purpose

Male Genital Desensitizer

Uses

• Helps in the prevention of premature ejaculation.

Warnings

For external use only.

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.

Avoid contact with the eyes.

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 Poision Control Center right away.

Directions

• Apply a small amount to the head and shaft of the penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

Other Information

• Store between 20-30ºC (68-86ºF)

Inactive ingredients

Alcohol, Propylene Glycol, PEG-8, Polysorbate 20, Phenoxyethanol, Ethylhexylglycerin, Cannabis Sativa Seed Oil

Package Labeling:

INGREDIENTS AND APPEARANCE

THUNDER FCK MALE GENITAL DESENSITIZER 
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70742-587
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	75 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70742-587-00	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/13/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/13/2025

Labeler - PRODUCT MAX GROUP INC (134893911)