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Pain Relief CVS by CVS

Medically reviewed on December 20, 2017

Dosage form: liquid
Ingredients: Lidocaine 4g in 100mL
Labeler: CVS
NDC Code: 69842-049

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.

Drug Facts

Active ingredient                                                         Purpose
Lidocaine 4%................................................................External analgesic


 Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations

For external use only.

Flammable: Do not use while smoking or near heat or flame Do not use in large quantities, particularly over raw surfaces or blistered areas
When using this product
• keep out of eyes
• use only as directed.
• do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF.
Stop use and ask doctor if
• condition gets worse • symptoms last more than 7 days
• symptoms clear up and occur again in a few days

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

Directions • shake well • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor • to apply to face, spray into palm of hand and gently apply

Inactive ingredients

 Aloe Barbadensis Leaf Juice, SD Alcohol 40, Propylene Glycol, Glycerin,
Simethicone, Tocopheryl Acetate, Triethanolamine, Carbomer,
Diazolidinyl Urea, Methylparaben, Propylparaben, Disodium
Cocoamphodipropionate, Disodium EDTA

lidocaine 4% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-049
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine (LIDOCAINE) Lidocaine4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Diazolidinyl Urea 
Disodium Cocoamphodipropionate 
Propylene Glycol 
#Item CodePackage Description
1NDC:69842-049-05133 mL in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/31/2017
Labeler - CVS (062312574)
Registrant - Product Quest Mfg (927768135)
Product Quest Mfg927768135manufacture(69842-049)


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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.