LUBELIFE CLIMAX CONTROL DELAY- benzocaine spray 
CC Wellness LLC

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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Benzocaine 7.5%

Male Genital Desensitizer

Uses:

For external use only

Avoid contact with the eyes

Allergy alert: do not use this product if you are allergic (sensitive) to local anesthetics or any of the other listed ingredients

Do not use on broken or inflamed skin

Ask a doctor before use:

  • If your partner is pregnant
  • If you have or have had liver or kidney problems

Ask a doctor or pharmacist before use if you are already taking prescribed drugs

When using this product

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

Can be used for sexual intercourse and sex play when applied in accordance with usage instructions. Only use in accordance with the instructions, seek medical attention immediately in case of overdose.

Keep out of reach of children

Directions:

Other information:

Inactive Ingredients:

PEG-8, Propylene Glycol, Water (Aqua)

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Principal Display Panel

LUBELIFE CLIMAX CONTROL DELAY 
benzocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71683-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE7.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71683-005-011 in 1 BOX01/01/2022
1NDC:71683-005-0260 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B01/01/2022
Labeler - CC Wellness LLC (067692292)
Establishment
NameAddressID/FEIBusiness Operations
CC Wellness LLC067692292manufacture(71683-005)

Revised: 6/2022
Document Id: e1a98e6d-0c25-75b8-e053-2a95a90ad136
Set id: e1a98e6d-0c24-75b8-e053-2a95a90ad136
Version: 1
Effective Time: 20220617
 
CC Wellness LLC