SWISS NAVY ENDURANCERX- lidocaine spray

Swiss Navy EnduranceRx by

Drug Labeling and Warnings

Swiss Navy EnduranceRx by is a Otc medication manufactured, distributed, or labeled by MD Science Lab, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (per spray)

Lidocaine approx. 10mg

Purpose

Anesthetic

Use:

Helps in temporarily slowing the onset of 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 doctor.

• For topical use only.

Do not use

• if you or your partner are  allergic to Lidocaine or topical anesthetics.
• Keep away from fire and flame.
• Discontinue use if you or your partner develop a rash or irritation, such as burning or itching.
• If symptoms persist, consult a doctor.
• Do not spray on broken, irritated or sensitive skin.
• Avoid contact with eyes.
• For external use only.

Keep out of reach of children.

• If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Apply 3 or more sprays, not to exceed 10, to head and shaft of penis, 10 minutes before intercourse, or use as directed by a doctor Rub into the skin and immediately wash off any residue. Wash product off after intercourse.

INACTIVE INGREDIENTS:

Deionized Water, Alcohol, Denat., Glycerin, Aloe Barbadensis Leaf Juice Powder.

Package Labeling:

INGREDIENTS AND APPEARANCE

SWISS NAVY ENDURANCERX 
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69898-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69898-003-15	1 in 1 BOX	08/04/2017
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	08/04/2017

Labeler - MD Science Lab, LLC (054484289)