BONADUR- lidocaine spray 
WebRx Pharmacy Palace

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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BonaDur Spray for Men

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

Ask a doctor or pharmacist before use if

Do not use if:

Stop use and ask a doctor

Warnings:

For external use only.

When using this product

Indications and Usage

Helps in temporarily slowing the onset of ejaculation.

Male genital desensitizing spray with lidocaine

Directions:

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:

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

Inactive Ingredients:

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

Questions?

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

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

OTC -Purpose

Anesthetic - Helps temporarily prolong the time until ejaculation

BonaDur ® For Men

BonaDurMale genital desensitizing spray with lidocaine

HELPS TEMPORARILY PROLONG THE TIME UNTIL EJACULATION

RAPID ACTING LIDOCAINE BASED FORMULA

Net Contents .25fl oz (7.4ml)

BONADUR 
lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70582-999
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS10 mg  in 1 mg
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
THYMOL (UNII: 3J50XA376E)  
SACCHARIN (UNII: FST467XS7D)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70582-999-741 in 1 BOX07/24/2015
110 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/24/2015
Labeler - WebRx Pharmacy Palace (136202699)
Establishment
NameAddressID/FEIBusiness Operations
WebRx Pharmacy Palace136202699manufacture(70582-999)

Revised: 11/2018
Document Id: 7b2018ec-84c3-6b95-e053-2a91aa0a2626
Set id: 2e879abe-03fc-71aa-e054-00144ff8d46c
Version: 4
Effective Time: 20181120
 
WebRx Pharmacy Palace