CVS BURN RELIEF W/LIDO 8OZ - lidocaine hcl gel 
CVS Pharmacy

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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Drug Facts

Active ingredient

Lidocaine HCl 0.5%


Purpose

Topical Analgesic


Uses

Warnings

For external use only

Do not use

in large quantities, particularly over raw surfaces or blistered areas.


When using this product

  • avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

  • irritation or rash develops
  • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

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

Directions

Inactive ingredients

Water, Propylene Glycol, Glycerin, Isopropyl Alcohol, Triethanolamine, Polysorbate 80, Carbomer, Aloe Barbadensis Leaf Juice Powder, Menthol, Disodium EDTA, Diazolidinyl Urea, Yellow 5, Blue 1.

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Compare to Solarcaine

Burn Relief Gel

NEW!

BURN RELIEF GEL

WITH LIDOCAINE HCl

RESTORES MOISTURE



NET WT 8 OZ (226 g)



Label





CVS BURN RELIEF W/LIDO 8OZ 
lidocaine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-670
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
TROLAMINE (UNII: 9O3K93S3TK)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-670-16226 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/08/2015
Labeler - CVS Pharmacy (062312574)

Revised: 3/2016
Document Id: 6fa8c6d5-fb6f-4b1f-8672-4ec8389bd57b
Set id: 36951b55-c8bb-4100-98e3-9a39fdcb76ea
Version: 2
Effective Time: 20160323
 
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