SWISS NAVY Endurance Rx

Manufacturer
PACKAGE SOLUTIONS LLC
Effective date
2023-10-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:23:51

Label at a glance#

ProductSWISS NAVY Endurance Rx
Active ingredientLIDOCAINE
Label structure6 sections

Dosage and administration

Apply 3 or more sprays, not to exceed to 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.

Label contents#

Full prescribing information#

Active Ingredients (per spray)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine approx. 10mg

Purpose

OTC - PURPOSE SECTION

Anesthetic

Use:

INDICATIONS & USAGE SECTION

Helps in temporarily slowing the onset of ejaculation.

WARNINGS:

WARNINGS SECTION

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 

OTC - DO NOT USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Apply 3 or more sprays, not to exceed to 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:

INACTIVE INGREDIENT SECTION

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

Packgae Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69872-00369872-003-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
289d047d-b161-495e-e063-6394a90ade797f193188-bdb3-401d-8dc7-cbd55e3d65ca2024-12-06WarningsExact identifier
spl set id: 7f193188-bdb3-401d-8dc7-cbd55e3d65ca

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.