BonaDur Spray for Men

Manufacturer
WebRx Pharmacy Palace
Effective date
2018-11-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:57:19

Label at a glance#

ProductBonaDur
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure14 sections

Indications and uses

Helps in temporarily slowing the onset of ejaculation. Male genital desensitizing spray with lidocaine

Dosage and administration

Remove plastic cap. Press the actuator repeatedly until product dispenses to prime spray pump. Apply 3 or more sprays not to exceed 10 to the head and shaft of the penis 10 minutes before sexual intercourse or use as directed by a doctor. Recommended initial dosage: 3 sprays. Rub BonaDur into the skin of the penis until all of the product is absorbed. Wash product off after intercourse. Replace plastic cap after e...

Storage and handling

Keep away from fire and flame. Store at 20°-25° C (68°-77° F).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (per spray): Lidocaine approx. 10mg

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if

  • You have liver problems.

OTC - DO NOT USE SECTION

Do not use if:

  • You or your partner are allergic to lidocaine or topical anesthetics.
  • Your partner is or may become pregnant.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of Children.
  • If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor

  • if you or your partner develop a rash or irritation, such as burning or itching. If symptoms persist, consult a doctor.
  • 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.

Warnings:

WARNINGS SECTION

For external use only.

When using this product

  • Do not spray on broken, irritated or sensitive skin.
  • Avoid contact with the eyes.

Indications and Usage

INDICATIONS & USAGE SECTION

Helps in temporarily slowing the onset of ejaculation.

Male genital desensitizing spray with lidocaine

Directions:

DOSAGE & ADMINISTRATION SECTION

Remove plastic cap. Press the actuator repeatedly until product dispenses to prime spray pump. Apply 3 or more sprays not to exceed 10 to the head and shaft of the penis 10 minutes before sexual intercourse or use as directed by a doctor. Recommended initial dosage: 3 sprays. Rub BonaDur into the skin of the penis until all of the product is absorbed. Wash product off after intercourse. Replace plastic cap after each use.

Other Information:

STORAGE AND HANDLING SECTION

Keep away from fire and flame. Store at 20°-25° C (68°-77° F).

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Ethyl Alcohol, Propylene Glycol, Purified Water, Oil of Peppermint, Citric Acid, Thymol.

Questions?

OTC - QUESTIONS SECTION

Phone 1-877-797-2522 within the United States for reporting serious adverse events associated with use of the product.

INFORMATION FOR PATIENTS SECTION

To re-order this product or for product information please visit: www.BonaDur.com

OTC -Purpose

OTC - PURPOSE SECTION

Anesthetic - Helps temporarily prolong the time until ejaculation

BonaDur ® For Men

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BonaDurBonaDurMale genital desensitizing spray with lidocaine

HELPS TEMPORARILY PROLONG THE TIME UNTIL EJACULATION

RAPID ACTING LIDOCAINE BASED FORMULA

Net Contents .25fl oz (7.4ml)

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70582-999-742020-01-31C16284748780-19d75b9d0-e833-f424-e053-dadaa90a57ceBonaDur Spray for Men

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70582-999-74BonaDur10 mg in 1 BOTTLE, SPRAYSPRAY104
70582-999-74BonaDur1 in 1 BOXSPRAY14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70582-999BONADUR (LIDOCAINE) SPRAY [WEBRX PHARMACY PALACE]4Legacy NDC, 2 package rows20181121_2e879abe-03fc-71aa-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70582-99970582-999-74

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
7b2018ec-84c3-6b95-e053-2a91aa0a26262e879abe-03fc-71aa-e054-00144ff8d46c2018-11-20WarningsExact identifier
spl id: 7b2018ec-84c3-6b95-e053-2a91aa0a2626
spl set id: 2e879abe-03fc-71aa-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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