ENDURE MALE GENITAL DESENSITIZING- lidocaine hydrochloride spray

ENDURE Male Genital Desensitizing by

Drug Labeling and Warnings

ENDURE Male Genital Desensitizing by is a Otc medication manufactured, distributed, or labeled by Endure Holdings, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine HCl 10mg

Purpose

Topical Anesthetic

Uses:

To help prevention of premature ejaculation

Warnings

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 physician.

Avoid contact with eyes.

If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a physician.

Keep out of reach of children.

Avoid contact with eyes.

Directions:

Prior to sexual intercourse, apply 3-6 sprays to the head and the shaft of the penis, not to exceed 10 sprays, or use as directed by a physician.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Ethylhexylglycerin, Glycerin, Glycyrrhiza Glabra (Licorice) Root Extract, L-Arginine, Lepidium Meyenii (Maca) Root Extract, Panax Ginseng Root Extract, Phenoxyethanol, Serenoa Serrulata (Saw Palmetto) Fruit Extract.

SPL UNCLASSIFIED SECTION

Distributed by:

ENDURE HOLDINGS LLC

WWW.ENDUREHOLDINGS.COM

5602 MARQUESAS CIRCLE

STE 207

SARASOTA, FL 34233

Package Label

ENDURE

Male Genital

Desensitizing

Spray

Fast Acting

Lidocaine-Based

Formulation

Color-Less

Odor-Less

Discreet

WWW.ENDUREHOLDINGS.COM

Net Contents:

0.25 Oz.

INGREDIENTS AND APPEARANCE

ENDURE MALE GENITAL DESENSITIZING 
lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69614-370
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	10 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ARGININE (UNII: 94ZLA3W45F)
LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
ASIAN GINSENG (UNII: CUQ3A77YXI)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SAW PALMETTO (UNII: J7WWH9M8QS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69614-370-01	7.4 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/07/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	02/18/2015

Labeler - Endure Holdings, LLC (079693684)